Variant report

Variant rs368325939
Chromosome Location chr9:116847788-116847789
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116843000-116858800 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr9:116844800-116851800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr9:116844800-116855400 Weak transcription Gastric stomach
4 chr9:116845200-116849000 Enhancers HepG2 liver
5 chr9:116845200-116850000 Weak transcription Fetal Lung lung
6 chr9:116845200-116854200 Weak transcription Pancreas Pancrea
7 chr9:116845200-116854600 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr9:116845200-116855000 Weak transcription Duodenum Mucosa Duodenum
9 chr9:116846200-116848000 Weak transcription Fetal Intestine Small intestine
10 chr9:116846200-116854400 Weak transcription Liver Liver
11 chr9:116847000-116853200 Weak transcription Fetal Intestine Large intestine
12 chr9:116847400-116848400 Weak transcription A549 lung
13 chr9:116847400-116856400 Weak transcription Fetal Kidney kidney
14 chr9:116847600-116848200 Bivalent Enhancer Fetal Muscle Trunk muscle

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