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

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Chromatin state (count:3 , 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
3	chr2:115750000-115750600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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