Variant report

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

rs_ID	r²[population]
rs61782625	1.00[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	nsv428466	chr1:70306638-70455357	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr1:70324000-70325200	Enhancers	HUVEC	blood vessel
2	chr1:70324800-70328400	Weak transcription	Muscle Satellite Cultured Cells	--

Quick Search:

Input of quick search could be: