Variant report

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

rs_ID	r²[population]
rs62485096	0.87[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	nsv888925	chr7:104047599-104170560	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104109000-104110000	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr7:104109200-104109800	Enhancers	Fetal Intestine Large	intestine

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