Variant report

Variant rs555152437
Chromosome Location chr9:116854604-116854605
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr9:116845200-116855000 Weak transcription Duodenum Mucosa Duodenum
4 chr9:116847400-116856400 Weak transcription Fetal Kidney kidney
5 chr9:116849000-116858800 Weak transcription HepG2 liver
6 chr9:116850600-116856800 Weak transcription Sigmoid Colon Sigmoid Colon
7 chr9:116851200-116857400 Strong transcription Fetal Intestine Small intestine
8 chr9:116853000-116858600 Strong transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr9:116853200-116858400 Strong transcription Fetal Intestine Large intestine
10 chr9:116854000-116857200 Strong transcription Fetal Stomach stomach
11 chr9:116854000-116858600 Weak transcription iPS-15b Cell Line embryonic stem cell
12 chr9:116854200-116858600 Strong transcription Pancreas Pancrea
13 chr9:116854400-116857000 Weak transcription Rectal Mucosa Donor 29 rectum
14 chr9:116854400-116858200 Strong transcription Liver Liver
15 chr9:116854600-116857000 Strong transcription Breast Myoepithelial Primary Cells Breast

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