Variant report

Variant rs72760611
Chromosome Location chr9:116833379-116833380
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr9:116832400-116835400 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr9:116832400-116835400 Enhancers Esophagus oesophagus
6 chr9:116832800-116833600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr9:116832800-116833600 Weak transcription Fetal Intestine Small intestine
8 chr9:116832800-116833800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr9:116833000-116833400 Weak transcription Fetal Intestine Large intestine
10 chr9:116833000-116833800 Enhancers HMEC breast
11 chr9:116833200-116833600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr9:116833200-116833600 Enhancers NHEK skin
13 chr9:116833200-116834000 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr9:116833200-116834000 Bivalent Enhancer Fetal Muscle Trunk muscle
15 chr9:116833200-116835400 Enhancers Fetal Muscle Leg muscle

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