Variant report

Variant rs28616789
Chromosome Location chr9:116832989-116832990
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116822600-116833400 Genic enhancers HepG2 liver
2 chr9:116828600-116833400 Weak transcription Pancreas Pancrea
3 chr9:116831400-116836200 Genic enhancers Liver Liver
4 chr9:116832400-116833000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
5 chr9:116832400-116833000 Enhancers Fetal Intestine Large intestine
6 chr9:116832400-116833000 Enhancers Sigmoid Colon Sigmoid Colon
7 chr9:116832400-116835400 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr9:116832400-116835400 Enhancers Esophagus oesophagus
9 chr9:116832800-116833200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr9:116832800-116833600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr9:116832800-116833600 Weak transcription Fetal Intestine Small intestine
12 chr9:116832800-116833800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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