Variant report

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs11886317	0.92[AFR][1000 genomes]
rs11888188	0.83[AFR][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	nsv1012193	chr2:211684524-212072213	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr2:211879000-211880400	Enhancers	Liver	Liver
2	chr2:211879400-211879800	Enhancers	HepG2	liver

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