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	nsv1034989	chr8:36242017-36436244	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	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	chr8:36243000-36243400	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr8:36243000-36243600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr8:36243000-36243600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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