Variant report

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	nsv874917	chr2:115723034-115788593	ZNF genes & repeats Enhancers Weak transcription	n/a	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	chr2:115749800-115750200	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr2:115749800-115750600	Enhancers	H9 Cell Line	embryonic stem cell

Quick Search:

Input of quick search could be: