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	nsv516881	chr1:192206032-192215064	Enhancers	TF binding region Chromatin interactive 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	chr1:192213200-192213400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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