Variant report

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526506	chr2:72192369-72206006	Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
2	nsv963619	chr2:72202518-72216578	Enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:72201200-72202800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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