From a9ac6739a0e7aa0fc9813fb3624d88a8fa3b96b2 Mon Sep 17 00:00:00 2001
From: Anja Thormann <anja@ebi.ac.uk>
Date: Fri, 12 Feb 2016 17:14:48 +0000
Subject: [PATCH] new human variation test database

---
 .../homo_sapiens/variation/allele.txt         |   1 +
 .../homo_sapiens/variation/allele_code.txt    |   0
 .../variation/associate_study.txt             |   0
 .../homo_sapiens/variation/attrib.txt         | 337 ++++++++++++++++++
 .../homo_sapiens/variation/attrib_set.txt     | 247 +++++++++++++
 .../homo_sapiens/variation/attrib_type.txt    |  33 ++
 .../variation/compressed_genotype_region.txt  |   0
 .../variation/compressed_genotype_var.txt     |   0
 .../homo_sapiens/variation/coord_system.txt   |   0
 .../homo_sapiens/variation/display_group.txt  |   0
 .../homo_sapiens/variation/failed_allele.txt  |   0
 .../variation/failed_description.txt          |  19 +
 .../variation/failed_structural_variation.txt |   0
 .../variation/failed_variation.txt            |   0
 .../homo_sapiens/variation/genotype_code.txt  |   0
 .../homo_sapiens/variation/individual.txt     |   0
 .../variation/individual_synonym.txt          |   0
 .../variation/individual_type.txt             |   4 +
 .../homo_sapiens/variation/meta.txt           |   3 +
 .../homo_sapiens/variation/meta_coord.txt     |   3 +
 .../variation/motif_feature_variation.txt     |   0
 .../homo_sapiens/variation/phenotype.txt      |   2 +
 .../variation/phenotype_feature.txt           |   2 +
 .../variation/phenotype_feature_attrib.txt    |   0
 .../homo_sapiens/variation/population.txt     |   1 +
 .../variation/population_genotype.txt         |   0
 .../variation/population_structure.txt        |   0
 .../variation/population_synonym.txt          |   0
 .../protein_function_predictions.txt          |   0
 .../protein_function_predictions_attrib.txt   |   0
 .../homo_sapiens/variation/publication.txt    |   0
 .../homo_sapiens/variation/read_coverage.txt  |   0
 .../regulatory_feature_variation.txt          |   0
 .../homo_sapiens/variation/sample.txt         |   0
 .../variation/sample_genotype_multiple_bp.txt |   0
 .../variation/sample_population.txt           |   0
 .../homo_sapiens/variation/seq_region.txt     |   1 +
 .../homo_sapiens/variation/source.txt         |   1 +
 .../variation/strain_gtype_poly.txt           |   0
 .../variation/structural_variation.txt        |   3 +
 .../structural_variation_association.txt      |   0
 .../structural_variation_feature.txt          |   3 +
 .../variation/structural_variation_sample.txt |   0
 .../homo_sapiens/variation/study.txt          |   1 +
 .../variation/submitter_handle.txt            |   0
 .../homo_sapiens/variation/subsnp_handle.txt  |   0
 .../variation/tagged_variation_feature.txt    |   0
 .../tmp_sample_genotype_single_bp.txt         |   0
 .../variation/transcript_variation.txt        |   0
 .../variation/translation_md5.txt             |   0
 .../homo_sapiens/variation/variation.txt      |   3 +
 .../variation/variation_attrib.txt            |   0
 .../variation/variation_citation.txt          |   0
 .../variation/variation_feature.txt           |   3 +
 .../variation/variation_genename.txt          |   0
 .../homo_sapiens/variation/variation_hgvs.txt |   0
 .../homo_sapiens/variation/variation_set.txt  |   1 +
 .../variation_set_structural_variation.txt    |   2 +
 .../variation/variation_set_structure.txt     |   0
 .../variation/variation_set_variation.txt     |   2 +
 .../variation/variation_synonym.txt           |   0
 61 files changed, 672 insertions(+)
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/allele.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/allele_code.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/associate_study.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/attrib.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/attrib_set.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/attrib_type.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/compressed_genotype_region.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/compressed_genotype_var.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/coord_system.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/display_group.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/failed_allele.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/failed_description.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/failed_structural_variation.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/failed_variation.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/genotype_code.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/individual.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/individual_synonym.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/individual_type.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/meta.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/meta_coord.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/motif_feature_variation.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/phenotype.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/phenotype_feature.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/phenotype_feature_attrib.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/population.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/population_genotype.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/population_structure.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/population_synonym.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/protein_function_predictions.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/protein_function_predictions_attrib.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/publication.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/read_coverage.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/regulatory_feature_variation.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/sample.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/sample_genotype_multiple_bp.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/sample_population.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/seq_region.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/source.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/strain_gtype_poly.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/structural_variation.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/structural_variation_association.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/structural_variation_feature.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/structural_variation_sample.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/study.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/submitter_handle.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/subsnp_handle.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/tagged_variation_feature.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/tmp_sample_genotype_single_bp.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/transcript_variation.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/translation_md5.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/variation.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/variation_attrib.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/variation_citation.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/variation_feature.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/variation_genename.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/variation_hgvs.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/variation_set.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/variation_set_structural_variation.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/variation_set_structure.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/variation_set_variation.txt
 create mode 100644 modules/t/test-genome-DBs/homo_sapiens/variation/variation_synonym.txt

diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/allele.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/allele.txt
new file mode 100644
index 0000000000..b662e7a1f9
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/allele.txt
@@ -0,0 +1 @@
+1	1	\N	0	1	0.8	\N	\N
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/allele_code.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/allele_code.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/associate_study.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/associate_study.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/attrib.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/attrib.txt
new file mode 100644
index 0000000000..06d6ff2926
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/attrib.txt
@@ -0,0 +1,337 @@
+2	2	SNV
+1	1	SO:0001483
+3	3	SNP
+5	2	substitution
+4	1	SO:1000002
+7	2	copy_number_variation
+6	1	SO:0001019
+8	3	CNV
+10	2	insertion
+9	1	SO:0000667
+12	2	deletion
+11	1	SO:0000159
+14	2	indel
+13	1	SO:1000032
+16	2	tandem_repeat
+15	1	SO:0000705
+18	2	sequence_alteration
+17	1	SO:0001059
+375	2	genetic_marker
+376	1	SO:0001645
+111	2	structural_variant
+112	1	SO:0001537
+113	3	SV
+114	2	probe
+115	1	SO:0000051
+116	3	CNV_PROBE
+200	2	copy_number_gain
+201	1	SO:0001742
+202	3	Gain
+203	2	copy_number_loss
+204	1	SO:0001743
+205	3	Loss
+206	2	inversion
+207	1	SO:1000036
+208	2	complex_structural_alteration
+209	1	SO:0001784
+210	3	Complex
+211	2	tandem_duplication
+212	1	SO:1000173
+213	3	Tandem duplication
+242	2	mobile_element_insertion
+243	1	SO:0001837
+244	3	Mobile element insertion
+286	2	interchromosomal_breakpoint
+287	1	SO:0001873
+288	3	Interchromosomal breakpoint
+289	2	intrachromosomal_breakpoint
+290	1	SO:0001874
+291	3	Intrachromosomal breakpoint
+292	2	translocation
+293	1	SO:0000199
+253	2	duplication
+254	1	SO:1000035
+331	3	Duplication
+361	2	novel_sequence_insertion
+362	1	SO:0001838
+363	3	Novel sequence insertion
+19	1	SO:0001628
+20	2	intergenic_variant
+294	6	38
+21	3	INTERGENIC
+118	5	transcript
+295	1	SO:0001631
+296	2	upstream_gene_variant
+266	6	24
+24	3	UPSTREAM
+297	1	SO:0001632
+298	2	downstream_gene_variant
+265	6	25
+27	3	DOWNSTREAM
+125	4	splice-5
+126	5	primary_transcript
+32	1	SO:0001575
+33	2	splice_donor_variant
+145	6	3
+34	3	ESSENTIAL_SPLICE_SITE
+128	4	splice-3
+129	1	SO:0001574
+36	2	splice_acceptor_variant
+37	1	SO:0001630
+38	2	splice_region_variant
+135	6	13
+39	3	SPLICE_SITE
+131	4	intron
+40	1	SO:0001627
+41	2	intron_variant
+120	6	21
+42	3	INTRONIC
+133	4	untranslated_5
+134	5	mRNA
+43	1	SO:0001623
+44	2	5_prime_UTR_variant
+122	6	18
+45	3	5PRIME_UTR
+136	4	untranslated_3
+46	1	SO:0001624
+47	2	3_prime_UTR_variant
+124	6	19
+48	3	3PRIME_UTR
+139	4	cds-synon
+299	1	SO:0001819
+300	2	synonymous_variant
+132	6	15
+54	3	SYNONYMOUS_CODING
+141	4	missense
+55	1	SO:0001583
+301	2	missense_variant
+153	6	12
+57	3	NON_SYNONYMOUS_CODING
+302	1	SO:0001821
+303	2	inframe_insertion
+140	6	10
+304	1	SO:0001822
+305	2	inframe_deletion
+154	6	11
+144	4	nonsense
+62	1	SO:0001587
+63	2	stop_gained
+146	6	4
+64	3	STOP_GAINED
+65	1	SO:0001578
+66	2	stop_lost
+143	6	6
+67	3	STOP_LOST
+68	1	SO:0001567
+69	2	stop_retained_variant
+70	1	SO:0002012
+306	2	start_lost
+142	6	7
+147	4	frameshift
+72	1	SO:0001589
+73	2	frameshift_variant
+138	6	5
+74	3	FRAMESHIFT_CODING
+75	1	SO:0001626
+76	2	incomplete_terminal_codon_variant
+137	6	14
+77	3	PARTIAL_CODON
+78	1	SO:0001621
+79	2	NMD_transcript_variant
+262	6	22
+80	3	NMD_TRANSCRIPT
+150	5	ncRNA
+81	1	SO:0001619
+82	2	non_coding_transcript_variant
+263	6	23
+83	3	WITHIN_NON_CODING_GENE
+307	1	SO:0001792
+308	2	non_coding_transcript_exon_variant
+119	6	20
+152	5	miRNA
+84	1	SO:0001620
+85	2	mature_miRNA_variant
+151	6	17
+86	3	WITHIN_MATURE_miRNA
+87	1	SO:0001580
+88	2	coding_sequence_variant
+149	6	16
+89	3	CODING_UNKNOWN
+155	5	regulatory_region
+90	1	SO:0001566
+91	2	regulatory_region_variant
+309	6	36
+92	3	REGULATORY_REGION
+157	5	TF_binding_site
+158	1	SO:0001782
+159	2	TF_binding_site_variant
+310	6	30
+311	1	SO:0001893
+312	2	transcript_ablation
+127	6	1
+313	1	SO:0001889
+314	2	transcript_amplification
+130	6	8
+315	1	SO:0001895
+316	2	TFBS_ablation
+261	6	26
+317	1	SO:0001892
+318	2	TFBS_amplification
+319	6	28
+320	1	SO:0001894
+321	2	regulatory_region_ablation
+322	6	31
+323	1	SO:0001891
+324	2	regulatory_region_amplification
+325	6	33
+346	5	sequence_feature
+326	1	SO:0001907
+327	2	feature_elongation
+328	1	SO:0001906
+329	2	feature_truncation
+330	6	37
+416	1	SO:0001818
+417	2	protein_altering_variant
+98	2	mRNA
+97	1	SO:0000234
+100	2	transcript
+99	1	SO:0000673
+102	2	primary_transcript
+101	1	SO:0000185
+104	2	ncRNA
+103	1	SO:0000655
+106	2	miRNA
+105	1	SO:0000276
+108	2	regulatory_region
+107	1	SO:0005836
+110	2	binding_site
+109	1	SO:0000409
+255	2	sequence_feature
+256	1	SO:0000110
+377	420	uncertain significance
+378	420	not provided
+379	420	benign
+380	420	likely benign
+381	420	likely pathogenic
+382	420	pathogenic
+383	420	drug response
+384	420	histocompatibility
+385	420	other
+386	420	confers sensitivity
+387	420	risk factor
+388	420	association
+389	420	protective
+215	10	unknown
+216	10	untested
+217	10	non-pathogenic
+218	10	probable-non-pathogenic
+219	10	probable-pathogenic
+220	10	pathogenic
+221	10	drug-response
+222	10	histocompatibility
+223	10	other
+176	9	hapmap
+177	9	ind_venter
+178	9	ind_watson
+179	9	fail_all
+180	9	fail_nonref
+181	9	fail_ambig
+182	9	fail_gt_fq
+183	9	fail_incons_map
+184	9	fail_mult_map
+185	9	fail_no_alleles
+186	9	fail_no_gt
+187	9	fail_no_map
+188	9	fail_no_seq
+189	9	fail_non_nt
+190	9	fail_mult_alleles
+214	9	fail_dbsnp_suspect
+191	9	ph_hgmd_pub
+193	9	ph_nhgri
+194	9	ph_omim
+195	9	ph_variants
+196	9	ph_uniprot
+197	9	ph_cosmic
+198	9	ph_ega
+257	9	hapmap_ceu
+258	9	hapmap_hcb
+259	9	hapmap_jpt
+260	9	hapmap_yri
+332	9	Affy_500K
+333	9	Affy_SNP6
+337	9	Cardio-Metabo_Chip
+338	9	HumanOmni1-Quad
+335	9	Illumina_1M-duo
+334	9	Illumina_660Q
+339	9	Illumina_CytoSNP12v1
+342	9	Human610_Quad
+343	9	HumanHap550
+340	9	HumanHap650Y
+341	9	HumanOmni2.5
+245	9	PorcineSNP60
+344	9	esp_6500
+345	9	clin_assoc
+360	9	all_chips
+348	9	Chicken600K
+349	9	EquineSNP50
+350	9	BovineHD
+351	9	BovineLD
+352	9	BovineSNP50
+355	9	phencode
+354	9	HumanOmni5
+356	9	OvineSNP50
+357	9	OvineHDSNP
+358	9	ExomeChip
+359	9	ImmunoChip
+373	9	HumanOmniExpress
+374	9	ClinVar
+353	9	MGP
+390	9	HumanCoreExome
+404	9	1kg_3
+405	9	1kg_3_afr
+406	9	1kg_3_amr
+407	9	1kg_3_eas
+408	9	1kg_3_sas
+409	9	1kg_3_eur
+410	9	1kg_3_com
+411	9	1kg_3_afr_com
+412	9	1kg_3_amr_com
+413	9	1kg_3_eas_com
+414	9	1kg_3_sas_com
+415	9	1kg_3_eur_com
+395	9	LSDB
+396	9	dbPEX
+397	9	HbVar
+398	9	Infevers
+399	9	KAT6BDB
+400	9	LMDD
+401	9	OIVD
+402	9	PAHdb
+270	8	tolerated
+271	8	deleterious
+391	8	tolerated - low confidence
+392	8	deleterious - low confidence
+272	7	probably damaging
+273	7	possibly damaging
+274	7	benign
+275	7	unknown
+267	12	sift
+268	12	polyphen_humvar
+269	12	polyphen_humdiv
+224	11	Not tested
+225	11	Benign
+226	11	Pathogenic
+227	11	Uncertain Significance
+228	11	likely benign
+229	11	likely pathogenic
+364	11	not provided
+365	11	association
+366	11	risk factor
+367	419	Multiple_observations
+368	419	Frequency
+369	419	HapMap
+370	419	1000Genomes
+371	419	Cited
+372	419	ESP
+418	419	Phenotype_or_Disease
+421	419	ExAC
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/attrib_set.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/attrib_set.txt
new file mode 100644
index 0000000000..b36010e2e2
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/attrib_set.txt
@@ -0,0 +1,247 @@
+1	1
+1	2
+1	3
+2	4
+2	5
+3	6
+3	7
+3	8
+4	9
+4	10
+5	11
+5	12
+6	13
+6	14
+7	15
+7	16
+8	17
+8	18
+38	97
+38	98
+39	99
+39	100
+40	101
+40	102
+41	103
+41	104
+42	105
+42	106
+43	107
+43	108
+44	109
+44	110
+45	111
+45	112
+45	113
+46	114
+46	115
+46	116
+49	200
+49	201
+49	202
+50	203
+50	204
+50	205
+51	206
+51	207
+52	208
+52	209
+52	210
+53	211
+53	212
+53	213
+54	242
+54	243
+54	244
+60	255
+60	256
+79	72
+79	73
+79	74
+79	134
+79	138
+79	147
+87	286
+87	287
+87	288
+88	289
+88	290
+88	291
+89	292
+89	293
+90	19
+90	20
+90	21
+90	294
+91	24
+91	118
+91	266
+91	295
+91	296
+92	27
+92	118
+92	265
+92	297
+92	298
+93	32
+93	33
+93	34
+93	125
+93	126
+93	145
+94	34
+94	36
+94	126
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diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/attrib_type.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/attrib_type.txt
new file mode 100644
index 0000000000..7dfc202f63
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/attrib_type.txt
@@ -0,0 +1,33 @@
+1	SO_accession		Sequence Ontology accession
+2	SO_term		Sequence Ontology term
+3	display_term		Ensembl display term
+4	NCBI_term		NCBI term
+5	feature_SO_term		Sequence Ontology term for the associated feature
+6	rank		Relative severity of this variation consequence
+7	polyphen_prediction		PolyPhen-2 prediction
+8	sift_prediction		SIFT prediction
+9	short_name	Short name	A shorter name for an instance, e.g. a VariationSet
+10	dbsnp_clin_sig	dbSNP/ClinVar clinical significance	The clinical significance of a variant as reported by ClinVar and dbSNP
+11	dgva_clin_sig	DGVa clinical significance	The clinical significance of a structural variant as reported by DGVa
+420	clinvar_clin_sig	ClinVar clinical significance	The clinical significance of a variant as reported by ClinVar
+12	prot_func_analysis	Protein function analysis 	The program used to make protein function predictions
+13	associated_gene	Associated gene	ID of gene(s) linked by phenotype association
+14	risk_allele	Risk allele	Risk allele in phenotype association
+15	p_value	P-value	P-value denoting significance of an observed phenotype annotation
+16	variation_names	Variation names	Variant ID(s) linked with a phenotype association
+17	sample_id	Sample ID	Sample ID for source of phenotype association
+18	strain_id	Strain ID	Strain ID for source of phenotype association
+19	lod_score	LOD score	Log Of Odds score
+20	variance	Variance	Variance statistic
+21	inheritance_type	Inheritance type	Inheritance type of a trait
+22	external_id	External ID	External identifier for an entity
+23	odds_ratio	Odds ratio	Odds ratio used to denote significance of an observed phenotype annotation
+24	beta_coef	Beta coefficient	Beta coefficient (or standardized coefficient) used to denote significance of an observed phenotype annotation
+25	allele_symbol	Allele symbol	Allele symbol linked with phenotype association
+26	allele_accession_id	Allele accession ID	Allele accession ID linked with phenotype association
+33	marker_accession_id	Marker accession ID	Marker ID linked with phenotype association
+419	evidence	Variant evidence status	Evidence status for a variant
+422	sequence_number	Number of sequences in alignment	Number of protein sequences in the alignment use to make a protein impact prediction
+423	based_on	Evidence type used for protein impact prediction	Evidence type used for a PolyPhen protein impact prediction
+424	conservation_score	Sift conservation score	Median conservation value in an alignment used to make a Sift prediction
+421	review_status	ClinVar review_status	ClinVar review_status for assertation
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/compressed_genotype_region.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/compressed_genotype_region.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/compressed_genotype_var.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/compressed_genotype_var.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/coord_system.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/coord_system.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/display_group.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/display_group.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/failed_allele.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/failed_allele.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/failed_description.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/failed_description.txt
new file mode 100644
index 0000000000..7e8600477f
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/failed_description.txt
@@ -0,0 +1,19 @@
+1	Variant maps to more than 3 different locations
+2	None of the variant alleles match the reference allele
+3	Variant has more than 3 different alleles
+4	Loci with no observed variant alleles in dbSNP
+5	Variant does not map to the genome
+6	Variant has no genotypes
+7	Genotype frequencies do not add up to 1
+8	Variant has no associated sequence
+9	Variant submission has been withdrawn by the 1000 genomes project due to high false positive rate
+11	Additional submitted allele data from dbSNP does not agree with the dbSNP refSNP alleles
+12	Variant has more than 3 different submitted alleles
+13	Alleles contain non-nucleotide characters
+14	Alleles contain ambiguity codes
+15	Mapped position is not compatible with reported alleles
+16	Flagged as suspect by dbSNP
+17	Variant can not be re-mapped to the current assembly
+18	Supporting evidence can not be re-mapped to the current assembly
+19	Variant maps to more than one genomic location
+20	Variant at first base in sequence
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/failed_structural_variation.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/failed_structural_variation.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/failed_variation.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/failed_variation.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/genotype_code.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/genotype_code.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/individual.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/individual.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/individual_synonym.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/individual_synonym.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/individual_type.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/individual_type.txt
new file mode 100644
index 0000000000..6da0c3ddd1
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/individual_type.txt
@@ -0,0 +1,4 @@
+1	fully_inbred	multiple organisms have the same genome sequence
+2	partly_inbred	single organisms have reduced genome variability due to human intervention
+3	outbred	a single organism which breeds freely
+4	mutant	a single or multiple organisms with the same genome sequence that have a natural or experimentally induced mutation
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/meta.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/meta.txt
new file mode 100644
index 0000000000..a1df78dac3
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/meta.txt
@@ -0,0 +1,3 @@
+1	\N	schema_type	variation
+2	\N	schema_version	84
+3	\N	patch	patch_83_84_a.sql|schema version
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/meta_coord.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/meta_coord.txt
new file mode 100644
index 0000000000..1d044f1d37
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/meta_coord.txt
@@ -0,0 +1,3 @@
+variation_feature	1	1000002
+structural_variation_feature	1	1000002
+phenotype_feature	1	1000002
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/motif_feature_variation.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/motif_feature_variation.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/phenotype.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/phenotype.txt
new file mode 100644
index 0000000000..5d21f089e7
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/phenotype.txt
@@ -0,0 +1,2 @@
+1	\N	phenotype	\N
+2	\N	phenotype2	\N
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/phenotype_feature.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/phenotype_feature.txt
new file mode 100644
index 0000000000..a2a651ab66
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/phenotype_feature.txt
@@ -0,0 +1,2 @@
+1	1	1	\N	Variation	rs12345	1	469283	30252800	30252800	1
+2	2	1	\N	Variation	rs54321	1	469283	30253900	30253900	1
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/phenotype_feature_attrib.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/phenotype_feature_attrib.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/population.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/population.txt
new file mode 100644
index 0000000000..ed8e12cf23
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/population.txt
@@ -0,0 +1 @@
+1	population	\N	\N	0	\N	UNDISPLAYABLE	\N
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/population_genotype.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/population_genotype.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/population_structure.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/population_structure.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/population_synonym.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/population_synonym.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/protein_function_predictions.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/protein_function_predictions.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/protein_function_predictions_attrib.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/protein_function_predictions_attrib.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/publication.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/publication.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/read_coverage.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/read_coverage.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/regulatory_feature_variation.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/regulatory_feature_variation.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/sample.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/sample.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/sample_genotype_multiple_bp.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/sample_genotype_multiple_bp.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/sample_population.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/sample_population.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/seq_region.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/seq_region.txt
new file mode 100644
index 0000000000..5411299b20
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/seq_region.txt
@@ -0,0 +1 @@
+469283	20	1
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/source.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/source.txt
new file mode 100644
index 0000000000..aa9041585a
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/source.txt
@@ -0,0 +1 @@
+1	dbSNP	\N	\N	\N	\N	germline	\N
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/strain_gtype_poly.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/strain_gtype_poly.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/structural_variation.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/structural_variation.txt
new file mode 100644
index 0000000000..9baa3c0d86
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/structural_variation.txt
@@ -0,0 +1,3 @@
+1	nsv12345	\N	1	\N	208	\N	\N	0	0	\N
+2	nsv67890	\N	1	\N	208	\N	\N	0	1	\N
+3	nsv09876	\N	1	\N	114	\N	\N	0	0	\N
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/structural_variation_association.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/structural_variation_association.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/structural_variation_feature.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/structural_variation_feature.txt
new file mode 100644
index 0000000000..02ddd82bd3
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/structural_variation_feature.txt
@@ -0,0 +1,3 @@
+1	469283	\N	30253000	\N	\N	30254000	\N	1	1	nsv12345	1	1	208	\N	0	0	\N	\N	1
+2	469283	\N	30255000	\N	\N	30256000	\N	1	2	nsv67890	1	1	208	\N	0	1	\N	\N	1
+3	469283	\N	30257000	\N	\N	30258000	\N	1	3	nsv09876	1	1	114	\N	0	0	\N	\N	
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/structural_variation_sample.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/structural_variation_sample.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/study.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/study.txt
new file mode 100644
index 0000000000..fbb110ae38
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/study.txt
@@ -0,0 +1 @@
+1	1	study_name	\N	\N	\N	\N
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/submitter_handle.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/submitter_handle.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/subsnp_handle.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/subsnp_handle.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/tagged_variation_feature.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/tagged_variation_feature.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/tmp_sample_genotype_single_bp.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/tmp_sample_genotype_single_bp.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/transcript_variation.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/transcript_variation.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/translation_md5.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/translation_md5.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/variation.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/variation.txt
new file mode 100644
index 0000000000..b944dfdf8d
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/variation.txt
@@ -0,0 +1,3 @@
+1	1	rs12345	\N	\N	0	0	\N	\N	\N	\N	\N	1
+2	1	rs67890	\N	\N	0	0	\N	\N	\N	\N	\N	1
+3	1	rs54321	\N	\N	0	1	\N	\N	\N	\N	\N	1
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/variation_attrib.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/variation_attrib.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/variation_citation.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/variation_citation.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/variation_feature.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/variation_feature.txt
new file mode 100644
index 0000000000..aea759c0f4
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/variation_feature.txt
@@ -0,0 +1,3 @@
+1	469283	30252800	30252800	1	1	\N	rs12345	1	genotyped	1	intergenic_variant	1	0	0	\N	\N	\N	\N	\N	\N	1
+2	469283	30252900	30252900	1	2	\N	rs67890	1	\N	1	intergenic_variant	1	0	0	\N	\N	\N	\N	\N	\N	1
+3	469283	30253900	30253900	1	3	\N	rs54321	1	\N	1	intergenic_variant		0	1	\N	\N	\N	\N	\N	\N	1
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/variation_genename.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/variation_genename.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/variation_hgvs.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/variation_hgvs.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/variation_set.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/variation_set.txt
new file mode 100644
index 0000000000..7e4abf84fc
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/variation_set.txt
@@ -0,0 +1 @@
+1	variation_set	\N	\N
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/variation_set_structural_variation.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/variation_set_structural_variation.txt
new file mode 100644
index 0000000000..e8d2c31aa1
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/variation_set_structural_variation.txt
@@ -0,0 +1,2 @@
+1	1
+2	1
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/variation_set_structure.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/variation_set_structure.txt
new file mode 100644
index 0000000000..e69de29bb2
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/variation_set_variation.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/variation_set_variation.txt
new file mode 100644
index 0000000000..e8d2c31aa1
--- /dev/null
+++ b/modules/t/test-genome-DBs/homo_sapiens/variation/variation_set_variation.txt
@@ -0,0 +1,2 @@
+1	1
+2	1
diff --git a/modules/t/test-genome-DBs/homo_sapiens/variation/variation_synonym.txt b/modules/t/test-genome-DBs/homo_sapiens/variation/variation_synonym.txt
new file mode 100644
index 0000000000..e69de29bb2
-- 
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