Variant report

Variant rs181056885
Chromosome Location chr9:116853946-116853947
allele A/C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116843000-116858800 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr9:116844800-116855400 Weak transcription Gastric stomach
3 chr9:116845200-116854200 Weak transcription Pancreas Pancrea
4 chr9:116845200-116854600 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr9:116845200-116855000 Weak transcription Duodenum Mucosa Duodenum
6 chr9:116846200-116854400 Weak transcription Liver Liver
7 chr9:116847400-116856400 Weak transcription Fetal Kidney kidney
8 chr9:116849000-116858800 Weak transcription HepG2 liver
9 chr9:116850600-116856800 Weak transcription Sigmoid Colon Sigmoid Colon
10 chr9:116851200-116857400 Strong transcription Fetal Intestine Small intestine
11 chr9:116853000-116854000 Weak transcription Fetal Stomach stomach
12 chr9:116853000-116858600 Strong transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr9:116853200-116858400 Strong transcription Fetal Intestine Large intestine

Quick Search:


  
Input of quick search could be:

what's new

Quick links