Variant report

rSNPs within LD-proxies of this variant (count:9)

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	esv2763462	chr5:68295338-68307023	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68298000-68301600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr5:68300400-68301000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr5:68300600-68302800	Weak transcription	Fetal Lung	lung

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