Variant report

Variant	rs6907185
Chromosome Location	chr6:31844684-31844685
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31844613..31847430-chr6:31865372..31868871,3	MCF-7	breast:
2	chr6:31795540..31798054-chr6:31844082..31846588,3	K562	blood:
3	chr6:31711941..31713458-chr6:31842956..31845692,2	K562	blood:
4	chr6:31837893..31841462-chr6:31843957..31848091,5	MCF-7	breast:
5	chr6:31618887..31620702-chr6:31843664..31845751,2	MCF-7	breast:
6	chr6:31842997..31844783-chr6:31848909..31851075,2	MCF-7	breast:
7	chr6:31841958..31846970-chr6:31854324..31857490,7	K562	blood:
8	chr6:31843997..31846007-chr6:31863630..31865953,2	K562	blood:
9	chr6:31800194..31804653-chr6:31841439..31846611,7	MCF-7	breast:
10	chr6:31704865..31707598-chr6:31843405..31844974,2	MCF-7	breast:
11	chr6:31842912..31845071-chr6:31845254..31847943,4	MCF-7	breast:
12	chr6:31843698..31845468-chr6:31852206..31854707,3	MCF-7	breast:
13	chr6:31830131..31833248-chr6:31843364..31845400,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000204385	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000201823	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs2257331	0.84[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs2844451	0.82[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs34431565	0.92[ASN][1000 genomes]
rs35604230	0.81[AMR][1000 genomes]
rs544167	0.84[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs62395827	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs62395828	0.92[ASN][1000 genomes]
rs62395851	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6939227	0.89[AFR][1000 genomes]
rs7743807	0.89[AFR][1000 genomes]
rs7769158	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
2	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
3	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
4	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
5	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
6	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
7	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
8	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
9	nsv1033154	chr6:31550614-32009410	Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	326 gene(s)	inside rSNPs	diseases
10	nsv1017945	chr6:31609641-32481240	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
11	esv3428142	chr6:31615800-31881809	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
12	nsv884428	chr6:31728102-31870326	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
13	nsv462872	chr6:31778272-31864304	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
14	nsv601945	chr6:31778272-31864304	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
15	nsv601950	chr6:31785438-32492308	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
16	nsv601951	chr6:31785438-32496748	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
17	nsv601955	chr6:31785453-32484368	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
18	nsv601956	chr6:31785453-32492308	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
19	nsv462874	chr6:31794592-31864304	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
20	nsv601959	chr6:31794592-31864304	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
21	nsv884472	chr6:31813898-31870856	Weak transcription Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
22	nsv508399	chr6:31829474-31902423	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
23	nsv884474	chr6:31836055-31870326	Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
24	nsv462875	chr6:31838441-31907147	Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
25	nsv601960	chr6:31838441-31907147	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
26	nsv884475	chr6:31840625-31880320	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs6907185	SKIV2L	cis	Esophagus Muscularis	GTEx
rs6907185	HLA-DRA	cis	lymphoblastoid	seeQTL

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31830800-31845200	Weak transcription	Small Intestine	intestine
2	chr6:31831800-31845000	Weak transcription	Lung	lung
3	chr6:31832000-31856000	Weak transcription	Right Atrium	heart
4	chr6:31832400-31847400	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr6:31832400-31847600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr6:31832400-31847600	Weak transcription	NH-A	brain
7	chr6:31832400-31848200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr6:31832400-31850800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr6:31833000-31847400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr6:31833200-31864200	Weak transcription	Fetal Heart	heart
11	chr6:31833800-31847400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr6:31836400-31847600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:31836800-31847800	Weak transcription	Hela-S3	cervix
14	chr6:31837200-31844800	Weak transcription	Pancreas	Pancrea
15	chr6:31838400-31845200	Weak transcription	Right Ventricle	heart
16	chr6:31838600-31846200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr6:31839000-31845000	Weak transcription	Fetal Kidney	kidney
18	chr6:31839000-31847400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr6:31839000-31849000	Weak transcription	HSMM	muscle
20	chr6:31839200-31847000	Weak transcription	Osteobl	bone
21	chr6:31839200-31847400	Weak transcription	HSMMtube	muscle
22	chr6:31839200-31848800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr6:31839400-31845200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr6:31839400-31847400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr6:31839400-31847400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:31839400-31847400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr6:31839400-31847400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr6:31839400-31847400	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr6:31839400-31847600	Weak transcription	HMEC	breast
30	chr6:31839600-31844800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr6:31839600-31847000	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr6:31839600-31847600	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr6:31839800-31847000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr6:31839800-31847400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr6:31841000-31847400	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr6:31842200-31846200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr6:31842400-31847200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr6:31842600-31847200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr6:31842600-31847400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr6:31842800-31845800	Weak transcription	Placenta	Placenta
41	chr6:31842800-31847400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr6:31842800-31848800	Weak transcription	Primary hematopoietic stem cells	blood
43	chr6:31843000-31847400	Weak transcription	Colon Smooth Muscle	Colon
44	chr6:31843000-31847600	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr6:31843000-31848800	Weak transcription	K562	blood
46	chr6:31843200-31847400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr6:31843400-31847400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr6:31843600-31845000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr6:31843600-31847400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr6:31843800-31844800	Genic enhancers	Fetal Intestine Large	intestine

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