Variant report

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs1167655	0.89[AMR][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	esv3446943	chr3:159388471-159409743	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3449677	chr3:159397558-159399556	Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:159396600-159398000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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