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	esv10137	chr12:25455511-25469350	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	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	chr12:25454400-25456200	Enhancers	Placenta	Placenta
2	chr12:25454600-25455600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr12:25455000-25456200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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