Variant report

Variant rs530512104
Chromosome Location chr17:16503900-16503901
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:3 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:16502400-16504000 Enhancers Fetal Intestine Small intestine
2 chr17:16503400-16505000 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
3 chr17:16503600-16504200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin

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