Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs12533063	0.84[EUR][1000 genomes]
rs12668581	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1476898	0.84[EUR][1000 genomes]
rs1860857	0.84[EUR][1000 genomes]
rs2058264	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2191276	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2430023	0.88[EUR][1000 genomes]
rs2471202	0.84[EUR][1000 genomes]
rs2471206	0.84[EUR][1000 genomes]
rs3808171	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs55728082	0.83[EUR][1000 genomes]
rs56326140	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs60730410	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61594727	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61692498	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73218224	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73218225	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73218228	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73218230	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73218231	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73218232	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73218233	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73218235	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs740813	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7786557	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7793961	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017029	chr7:121958574-122338623	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv532178	chr7:122203056-122978846	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:122217600-122265600	Weak transcription	Aorta	Aorta
2	chr7:122231200-122246200	Weak transcription	Left Ventricle	heart
3	chr7:122237600-122258800	Weak transcription	Pancreas	Pancrea
4	chr7:122238000-122257200	Weak transcription	Fetal Lung	lung
5	chr7:122239400-122244200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr7:122240400-122256200	Weak transcription	Liver	Liver
7	chr7:122242800-122243200	Enhancers	Fetal Heart	heart

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