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	nsv521769	chr1:71578442-71633719	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	1 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	chr1:71582200-71582600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:71582200-71582600	Enhancers	Fetal Brain Male	brain
3	chr1:71582200-71583800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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