Variant report

Variant rs16912311
Chromosome Location chr9:116832540-116832541
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 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 chr9:116832000-116832600 Enhancers Rectal Mucosa Donor 31 rectum
5 chr9:116832200-116832600 Weak transcription Fetal Intestine Small intestine
6 chr9:116832400-116832800 Enhancers Colonic Mucosa Colon
7 chr9:116832400-116833000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
8 chr9:116832400-116833000 Enhancers Fetal Intestine Large intestine
9 chr9:116832400-116833000 Enhancers Sigmoid Colon Sigmoid Colon
10 chr9:116832400-116835400 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr9:116832400-116835400 Enhancers Esophagus oesophagus

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