Variant report

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3384168	chr6:121043302-121056680	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
2	esv3366823	chr6:121043302-121064055	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:121052800-121056600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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