Variant report

Variant rs563280616
Chromosome Location chr9:116846583-116846584
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116840000-116847000 Enhancers Fetal Intestine Large intestine
2 chr9:116843000-116858800 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr9:116844800-116851800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr9:116844800-116855400 Weak transcription Gastric stomach
5 chr9:116845000-116847200 Enhancers Fetal Stomach stomach
6 chr9:116845000-116847400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr9:116845200-116846800 Weak transcription Fetal Muscle Trunk muscle
8 chr9:116845200-116849000 Enhancers HepG2 liver
9 chr9:116845200-116850000 Weak transcription Fetal Lung lung
10 chr9:116845200-116854200 Weak transcription Pancreas Pancrea
11 chr9:116845200-116854600 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr9:116845200-116855000 Weak transcription Duodenum Mucosa Duodenum
13 chr9:116845400-116847400 Enhancers A549 lung
14 chr9:116846000-116847200 Enhancers Stomach Smooth Muscle stomach
15 chr9:116846200-116847600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr9:116846200-116848000 Weak transcription Fetal Intestine Small intestine
17 chr9:116846200-116854400 Weak transcription Liver Liver
18 chr9:116846400-116847400 Enhancers Fetal Kidney kidney

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