Variant report

Variant rs7853169
Chromosome Location chr9:116857165-116857166
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116843000-116858800 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr9:116849000-116858800 Weak transcription HepG2 liver
3 chr9:116851200-116857400 Strong transcription Fetal Intestine Small intestine
4 chr9:116853000-116858600 Strong transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr9:116853200-116858400 Strong transcription Fetal Intestine Large intestine
6 chr9:116854000-116857200 Strong transcription Fetal Stomach stomach
7 chr9:116854000-116858600 Weak transcription iPS-15b Cell Line embryonic stem cell
8 chr9:116854200-116858600 Strong transcription Pancreas Pancrea
9 chr9:116854400-116858200 Strong transcription Liver Liver
10 chr9:116854800-116859600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr9:116855000-116858400 Strong transcription Duodenum Mucosa Duodenum
12 chr9:116855000-116858800 Weak transcription HUES48 Cell Line embryonic stem cell
13 chr9:116855400-116858800 Strong transcription Gastric stomach
14 chr9:116855400-116859800 Weak transcription Lung lung
15 chr9:116855400-116859800 Weak transcription Rectal Mucosa Donor 31 rectum
16 chr9:116855800-116858600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
17 chr9:116856400-116858000 Strong transcription Fetal Kidney kidney
18 chr9:116856400-116859800 Weak transcription Brain Inferior Temporal Lobe brain
19 chr9:116857000-116857400 Strong transcription Rectal Mucosa Donor 29 rectum
20 chr9:116857000-116859200 Weak transcription Breast Myoepithelial Primary Cells Breast

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