Variant report

Variant rs41277733
Chromosome Location chr9:116839909-116839910
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116835400-116840200 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr9:116837200-116842400 Enhancers A549 lung
3 chr9:116838800-116840600 Active TSS Liver Liver
4 chr9:116838800-116840600 Bivalent/Poised TSS HepG2 liver
5 chr9:116839000-116841600 Enhancers Rectal Mucosa Donor 31 rectum
6 chr9:116839000-116845200 Enhancers Stomach Mucosa stomach
7 chr9:116839200-116840600 Bivalent/Poised TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr9:116839400-116840800 Enhancers Fetal Lung lung
9 chr9:116839600-116841200 Enhancers Gastric stomach
10 chr9:116839800-116840000 Bivalent Enhancer Duodenum Smooth Muscle Duodenum
11 chr9:116839800-116840800 Flanking Active TSS Pancreas Pancrea
12 chr9:116839800-116841000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr9:116839800-116841000 Enhancers Esophagus oesophagus
14 chr9:116839800-116841400 Enhancers Colonic Mucosa Colon
15 chr9:116839800-116841400 Enhancers Duodenum Mucosa Duodenum
16 chr9:116839800-116841800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr9:116839800-116846200 Enhancers Fetal Intestine Small intestine

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