Variant report

rSNPs within LD-proxies of this variant (count:4)

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	nsv981403	chr7:96934701-96946503	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
2	nsv1028319	chr7:96940309-97012717	Enhancers Weak transcription ZNF genes & repeats	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	chr7:96943200-96945600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:96943800-96947000	Weak transcription	H9 Cell Line	embryonic stem cell

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