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	nsv881635	chr5:30122190-30371238	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	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	chr5:30121400-30125200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr5:30122600-30123200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr5:30122800-30123000	Enhancers	HUES6 Cell Line	embryonic stem cell

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