Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10068757	0.86[ASN][1000 genomes]
rs11241277	0.86[ASN][1000 genomes]
rs163207	0.86[ASN][1000 genomes]
rs163209	0.86[ASN][1000 genomes]
rs163306	0.86[ASN][1000 genomes]
rs173991	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs337686	0.86[ASN][1000 genomes]
rs337688	0.86[ASN][1000 genomes]
rs337694	0.86[ASN][1000 genomes]
rs337696	0.86[ASN][1000 genomes]
rs337697	0.86[ASN][1000 genomes]
rs337698	0.86[ASN][1000 genomes]
rs337701	0.86[ASN][1000 genomes]
rs337702	0.86[ASN][1000 genomes]
rs337703	0.86[ASN][1000 genomes]
rs337706	0.86[ASN][1000 genomes]
rs337713	0.86[ASN][1000 genomes]
rs337715	0.86[ASN][1000 genomes]
rs337716	0.86[ASN][1000 genomes]
rs36937	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36940	1.00[ASN][1000 genomes]
rs36941	1.00[ASN][1000 genomes]
rs36943	1.00[ASN][1000 genomes]
rs36944	1.00[ASN][1000 genomes]
rs36948	0.86[ASN][1000 genomes]
rs402876	0.86[ASN][1000 genomes]
rs481248	1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882728	chr5:113651694-113731423	Bivalent/Poised TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr5:113664600-113666600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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