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	esv3426519	chr2:180514391-180514819	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

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Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180508400-180517000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:180512200-180514600	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr2:180512200-180516400	Weak transcription	Fetal Lung	lung
4	chr2:180513000-180517000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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