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	nsv508188	chr2:184353162-184383232	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	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	chr2:184351000-184360200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:184351200-184353400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:184351800-184355200	Enhancers	Fetal Heart	heart

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