Variant report

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

rs_ID	r²[population]
rs7157913	0.86[AMR][1000 genomes]
rs8022102	0.91[AMR][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	nsv1042953	chr14:63314591-63384260	Enhancers Weak transcription	Chromatin interactive region	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	chr14:63364000-63369200	Weak transcription	H1 Cell Line	embryonic stem cell

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