Variant report

Variant rs567290936
Chromosome Location chr5:1648402-1648403
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:4 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:1645800-1653000 Weak transcription Spleen Spleen
2 chr5:1648400-1648600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
3 chr5:1648400-1648600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
4 chr5:1648400-1649600 Enhancers NHDF-Ad bronchial

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