Variant report

Variant rs116937342
Chromosome Location chr9:116854176-116854177
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 chr9:116845200-116854200 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 chr9:116853000-116858600 Strong transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr9:116853200-116858400 Strong transcription Fetal Intestine Large intestine
13 chr9:116854000-116854400 Bivalent Enhancer Fetal Muscle Trunk muscle
14 chr9:116854000-116857200 Strong transcription Fetal Stomach stomach
15 chr9:116854000-116858600 Weak transcription iPS-15b Cell Line embryonic stem cell

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