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	nsv902160	chr14:84694867-84730585	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	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	chr14:84694400-84696000	Enhancers	HUVEC	blood vessel
2	chr14:84694800-84695200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:84695000-84695400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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