Variant report

Variant	rs7836381
Chromosome Location	chr8:91155583-91155584
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:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:91151874..91154123-chr8:91154645..91156445,2	K562	blood:
2	chr4:6564574..6566094-chr8:91155316..91156835,2	K562	blood:
3	chr8:91155035..91157497-chr8:91163156..91166027,2	K562	blood:
4	chr10:103124108..103124630-chr8:91155315..91155836,3	HCT-116	colon:
5	chr8:91152815..91155655-chr8:91173130..91176716,3	K562	blood:
6	chr11:62608625..62609221-chr8:91155315..91155835,7	Hela-S3	cervix:
7	chr8:91148105..91150746-chr8:91155344..91157015,2	K562	blood:
8	chr3:73159952..73160589-chr8:91154816..91155815,2	Hela-S3	cervix:
9	chr3:73160015..73161608-chr8:91155335..91156836,2	K562	blood:
10	chr11:62607647..62609221-chr8:91155335..91156835,2	MCF-7	breast:
11	chr17:41464289..41466075-chr8:91155315..91156816,2	MCF-7	breast:
12	chr11:62608628..62609154-chr8:91155316..91155836,3	MCF-7	breast:
13	chr11:62607627..62609222-chr8:91155315..91156836,3	K562	blood:
14	chr1:160080964..160082487-chr8:91155315..91156836,2	K562	blood:
15	chr3:73158464..73161607-chr8:91155315..91156835,5	K562	blood:
16	chr17:41463347..41467581-chr8:91153836..91156836,7	K562	blood:
17	chr3:73159863..73160626-chr8:91155316..91155835,2	MCF-7	breast:
18	chr17:41463347..41467815-chr8:91153835..91156835,9	K562	blood:
19	chr17:41465192..41465706-chr8:91155316..91155835,2	HCT-116	colon:
20	chr3:73159943..73160600-chr8:91154835..91155836,3	HCT-116	colon:
21	chr11:62608623..62609195-chr8:91155314..91155835,10	HCT-116	colon:
22	chr17:41400577..41402205-chr8:91155335..91156836,2	K562	blood:
23	chr11:62608628..62609148-chr8:91155315..91155836,4	NB4	blood:
24	chr3:73159863..73160591-chr8:91155335..91155835,3	MCF-7	breast:
25	chr17:41464201..41467636-chr8:91155335..91156835,3	MCF-7	breast:
26	chr11:62608620..62609200-chr8:91155315..91155835,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000223247	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000188825	Chromatin interaction
ENSG00000074211	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10504891	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12675530	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs16903927	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs16904011	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3758145	0.86[AMR][1000 genomes]
rs6982611	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6997558	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7001425	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7818433	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758164	chr8:91000786-91329669	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Active TSS 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	18 gene(s)	inside rSNPs	diseases
2	esv2759628	chr8:91000786-91329669	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	esv2757281	chr8:91090821-91235335	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	esv34347	chr8:91101339-91179126	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
5	nsv470225	chr8:91113616-91229254	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
6	nsv891184	chr8:91114698-91222654	Active TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
7	nsv824687	chr8:91144854-91177488	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
8	esv35109	chr8:91150726-91226940	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
9	nsv818643	chr8:91153308-91212148	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91155400-91156600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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