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	esv3414372	chr10:23677617-23677919	Enhancers Weak transcription	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	chr10:23671000-23679600	Weak transcription	Placenta	Placenta
2	chr10:23677400-23677800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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