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	nsv961361	chr2:180530964-180534513	Weak transcription Enhancers	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	chr2:180531800-180536400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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