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	nsv970064	chr6:145921494-145933513	Enhancers Weak transcription	Chromatin interactive region	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	chr6:145922000-145926000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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