Variant report

Variant	rs2911975
Chromosome Location	chr8:6589443-6589444
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:6582565..6584469-chr8:6589315..6591124,2	K562	blood:
2	chr8:6579053..6581015-chr8:6588545..6590944,2	MCF-7	breast:
3	chr8:6588695..6590536-chr8:6600051..6602655,2	K562	blood:
4	chr8:6563956..6568156-chr8:6584449..6592281,7	MCF-7	breast:
5	chr8:6565315..6567017-chr8:6588017..6590548,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000155189	Chromatin interaction
ENSG00000249898	Chromatin interaction

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10096753	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs10108451	0.84[CEU][hapmap]
rs10110103	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs1365041	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1365042	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs1365043	0.90[EUR][1000 genomes]
rs1559744	0.89[CEU][hapmap]
rs1559748	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs1961768	0.94[CHB][hapmap];0.94[JPT][hapmap];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1971312	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2059536	0.83[EUR][1000 genomes]
rs2408444	0.93[CEU][hapmap]
rs2911970	1.00[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs2911971	0.94[CHB][hapmap];0.81[AMR][1000 genomes]
rs2911976	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs2911977	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs2911978	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2911979	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2911980	0.96[CEU][hapmap];0.83[EUR][1000 genomes]
rs2911983	0.89[EUR][1000 genomes]
rs2911987	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2911992	0.85[ASN][1000 genomes]
rs2912050	0.85[JPT][hapmap]
rs2912054	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2912067	0.81[EUR][1000 genomes]
rs2928576	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2928579	1.00[CHB][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs2928617	0.83[EUR][1000 genomes]
rs2928618	0.91[EUR][1000 genomes]
rs2928619	0.91[EUR][1000 genomes]
rs2928621	0.91[EUR][1000 genomes]
rs2928623	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2928625	0.96[CEU][hapmap];0.83[EUR][1000 genomes]
rs2928626	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2928629	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2928630	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2928631	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2936502	0.93[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2936505	0.83[CHB][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs2936506	0.82[ASN][1000 genomes]
rs2936507	0.93[CHB][hapmap];0.85[JPT][hapmap];0.81[ASN][1000 genomes]
rs2936512	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2936520	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs2980658	0.83[AMR][1000 genomes]
rs2980679	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2980680	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2980682	0.84[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2980683	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs2980684	1.00[CEU][hapmap];0.89[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs2980686	0.88[EUR][1000 genomes]
rs2980688	0.93[CHB][hapmap];0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs2980689	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2980690	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2980692	0.93[EUR][1000 genomes]
rs3780087	0.92[CEU][hapmap]
rs6559178	0.87[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs7015837	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs71505132	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs992813	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021175	chr8:5965453-6880364	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv1027682	chr8:6018123-6920312	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv1027313	chr8:6286575-6920312	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv1021684	chr8:6350091-6809455	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	esv2422383	chr8:6362389-6781593	Enhancers Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv610004	chr8:6402366-6772913	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv1029241	chr8:6411300-6761720	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
8	nsv933075	chr8:6456475-7366650	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
9	nsv1025976	chr8:6472948-6686972	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
10	nsv933768	chr8:6482944-6618221	Strong transcription Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
11	nsv831220	chr8:6527845-6728491	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
12	nsv1030637	chr8:6545498-6669949	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
13	nsv1034115	chr8:6546984-6665832	Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
14	nsv465436	chr8:6568201-6921404	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
15	nsv610006	chr8:6568201-6921404	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
16	nsv1031063	chr8:6570354-6622685	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
17	nsv1027883	chr8:6570354-7250368	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
18	nsv1024685	chr8:6575334-6622685	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
19	nsv1034812	chr8:6578390-6920312	Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
20	nsv949532	chr8:6579563-6999220	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
21	nsv482865	chr8:6585920-6765111	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers Bivalent Enhancer Active TSS Strong transcription 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	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6567400-6590000	Weak transcription	Left Ventricle	heart
2	chr8:6567400-6590200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr8:6567400-6590600	Weak transcription	Psoas Muscle	Psoas
4	chr8:6567400-6590800	Weak transcription	Pancreas	Pancrea
5	chr8:6567400-6592600	Weak transcription	Aorta	Aorta
6	chr8:6567800-6590000	Weak transcription	NHLF	lung
7	chr8:6568000-6603400	Weak transcription	Fetal Brain Male	brain
8	chr8:6568400-6589800	Weak transcription	HSMMtube	muscle
9	chr8:6568400-6590400	Weak transcription	Brain Germinal Matrix	brain
10	chr8:6572400-6590000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr8:6576000-6589800	Weak transcription	Fetal Muscle Leg	muscle
12	chr8:6576000-6590800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:6576000-6590800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr8:6576000-6591200	Weak transcription	Fetal Stomach	stomach
15	chr8:6576200-6590200	Weak transcription	Fetal Heart	heart
16	chr8:6576200-6590400	Weak transcription	Fetal Brain Female	brain
17	chr8:6576400-6590200	Weak transcription	Brain Cingulate Gyrus	brain
18	chr8:6577200-6590000	Weak transcription	Thymus	Thymus
19	chr8:6577800-6592000	Weak transcription	Placenta	Placenta
20	chr8:6578200-6590600	Weak transcription	Fetal Muscle Trunk	muscle
21	chr8:6582600-6594600	Strong transcription	Hela-S3	cervix
22	chr8:6584400-6590000	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr8:6584800-6592200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr8:6585200-6590800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr8:6585600-6590000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr8:6585600-6590200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr8:6585600-6590800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr8:6585600-6591000	Weak transcription	Stomach Mucosa	stomach
29	chr8:6585800-6590800	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr8:6585800-6591800	Weak transcription	Fetal Intestine Small	intestine
31	chr8:6585800-6591800	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr8:6585800-6592400	Weak transcription	Colonic Mucosa	Colon
33	chr8:6585800-6592600	Weak transcription	Esophagus	oesophagus
34	chr8:6585800-6615800	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr8:6586600-6592200	Weak transcription	Ovary	ovary
36	chr8:6587000-6589800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr8:6587200-6589600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr8:6587200-6590200	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr8:6587200-6590200	Weak transcription	Osteobl	bone
40	chr8:6587200-6590400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr8:6587200-6590400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr8:6587200-6590400	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr8:6587200-6590800	Weak transcription	HMEC	breast
44	chr8:6587200-6590800	Weak transcription	NHDF-Ad	bronchial
45	chr8:6587200-6604600	Weak transcription	NHEK	skin
46	chr8:6587200-6617000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr8:6587400-6590400	Weak transcription	Adipose Nuclei	Adipose
48	chr8:6587400-6590600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr8:6587400-6590600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr8:6587600-6590200	Weak transcription	Primary T cells from cord blood	blood

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