Variant report

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3357488	chr14:83291024-83293572	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
2	esv3392705	chr14:83291124-83293547	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
3	esv3322199	chr14:83291499-83292897	Enhancers	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	chr14:83291400-83291600	Enhancers	H9 Cell Line	embryonic stem cell
2	chr14:83291400-83291800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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