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	nsv969415	chr6:64323751-64326310	Enhancers Weak transcription Active TSS	TF binding region	2 gene(s)	inside rSNPs	diseases

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Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:64324400-64326000	Weak transcription	K562	blood
2	chr6:64325400-64326200	Enhancers	H9 Cell Line	embryonic stem cell
3	chr6:64325400-64326200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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