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	esv3427167	chr10:23433696-23435794	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	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	chr10:23433000-23437200	Weak transcription	Pancreas	Pancrea
2	chr10:23433600-23434600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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