Variant report

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	nsv565333	chr14:83397783-83437617	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
2	nsv974470	chr14:83412606-83416274	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:83413200-83417200	Weak transcription	HUES64 Cell Line	embryonic stem cell

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