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	esv3395787	chr11:15491376-15493524	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

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Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15489400-15492600	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr11:15490600-15493000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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