Variant report

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv988081	chr2:184342009-184342583	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv9793	chr2:184342024-184342583	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3416805	chr2:184342157-184345105	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:184342400-184352600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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