Variant report

Variant	rs6469722
Chromosome Location	chr8:119140437-119140438
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10505328	0.84[EUR][1000 genomes]
rs10755915	0.86[CHD][hapmap];0.95[JPT][hapmap]
rs10808492	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs10808494	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs10955855	0.83[ASN][1000 genomes]
rs10955856	0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs10955857	0.85[EUR][1000 genomes]
rs11562678	0.86[EUR][1000 genomes]
rs11781739	0.89[CEU][hapmap];0.87[CHB][hapmap];0.87[EUR][1000 genomes]
rs12548404	0.87[ASN][1000 genomes]
rs12679263	0.89[CEU][hapmap];0.87[CHB][hapmap];0.87[EUR][1000 genomes]
rs13270513	0.81[JPT][hapmap]
rs3757991	0.88[CHD][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs4147528	0.89[CEU][hapmap];0.87[CHB][hapmap];0.91[TSI][hapmap];0.87[EUR][1000 genomes]
rs4876400	0.86[CHD][hapmap];0.95[JPT][hapmap]
rs4876791	0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs4876792	0.87[EUR][1000 genomes]
rs6469721	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs6469723	0.86[EUR][1000 genomes]
rs6991511	0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs6993268	0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs7008536	0.95[JPT][hapmap]
rs7010382	0.95[JPT][hapmap]
rs7011384	0.95[JPT][hapmap]
rs7014053	0.83[CHB][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs7818011	0.83[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs7835605	0.88[CHD][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs7835956	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs7837824	0.95[JPT][hapmap]
rs897828	0.95[JPT][hapmap]
rs897830	0.95[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030459	chr8:118840179-119155835	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv612047	chr8:118939094-119468609	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv1015380	chr8:118948652-119418389	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv539736	chr8:118948652-119418389	Flanking Active TSS Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv831441	chr8:119055370-119262970	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
6	nsv821660	chr8:119082062-119312183	Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119125800-119149600	Weak transcription	Aorta	Aorta
2	chr8:119139600-119146400	Weak transcription	Fetal Muscle Leg	muscle

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