Variant report

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

rs_ID	r²[population]
rs13398571	0.85[AFR][1000 genomes]
rs13404627	0.84[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	nsv875618	chr2:190789387-190883360	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region 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	chr2:190811400-190815200	Weak transcription	GM12878-XiMat	blood
2	chr2:190812000-190816400	Weak transcription	Primary B cells from cord blood	blood

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