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	esv2456671	chr4:147852567-147853859	Enhancers Weak transcription	TF binding region	1 gene(s)	inside rSNPs	diseases

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147853200-147853800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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