Variant report

Variant rs60017130
Chromosome Location chr9:116843497-116843498
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116839000-116845200 Enhancers Stomach Mucosa stomach
2 chr9:116839800-116846200 Enhancers Fetal Intestine Small intestine
3 chr9:116840000-116847000 Enhancers Fetal Intestine Large intestine
4 chr9:116840800-116844600 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr9:116840800-116845200 Enhancers Pancreas Pancrea
6 chr9:116841200-116843600 Weak transcription Lung lung
7 chr9:116841600-116845200 Enhancers Fetal Kidney kidney
8 chr9:116842400-116844800 Enhancers Gastric stomach
9 chr9:116842400-116844800 Enhancers Sigmoid Colon Sigmoid Colon
10 chr9:116842400-116845200 Flanking Active TSS Liver Liver
11 chr9:116842400-116845200 Enhancers Duodenum Mucosa Duodenum
12 chr9:116842600-116843800 Weak transcription Small Intestine intestine
13 chr9:116842600-116844800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr9:116842600-116845000 Enhancers Rectal Mucosa Donor 29 rectum
15 chr9:116843000-116843600 Weak transcription Fetal Lung lung
16 chr9:116843000-116845400 Enhancers Colonic Mucosa Colon
17 chr9:116843000-116858800 Weak transcription Pancreatic Islets Pancreatic Islet
18 chr9:116843200-116843600 Enhancers Rectal Mucosa Donor 31 rectum
19 chr9:116843200-116843600 Active TSS HepG2 liver
20 chr9:116843400-116844000 Flanking Active TSS A549 lung

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