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	nsv438136	chrX:66238345-66664219	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	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	chrX:66263600-66264000	Bivalent Enhancer	Adipose Nuclei	Adipose
2	chrX:66263600-66264000	Flanking Active TSS	Liver	Liver

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