Variant report

Variant rs6791444
Chromosome Location chr3:100402257-100402258
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100400200-100402600 Genic enhancers Fetal Intestine Small intestine
2 chr3:100401000-100402600 Strong transcription Primary neutrophils fromperipheralblood blood
3 chr3:100401600-100410600 Weak transcription Liver Liver
4 chr3:100401800-100402600 Flanking Active TSS HepG2 liver
5 chr3:100401800-100402800 Enhancers Fetal Intestine Large intestine
6 chr3:100402000-100402600 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr3:100402000-100403600 Weak transcription Pancreas Pancrea
8 chr3:100402200-100402600 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr3:100402200-100402600 Flanking Active TSS Duodenum Mucosa Duodenum

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