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	nsv524029	chr3:118154526-118157095	Enhancers Flanking Active TSS	n/a	n/a	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	chr3:118154600-118155000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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