Variant report

Variant rs13283334
Chromosome Location chr9:117531782-117531783
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:117525800-117533000 Weak transcription Aorta Aorta
2 chr9:117529400-117532600 Enhancers Fetal Intestine Large intestine
3 chr9:117529800-117533400 Weak transcription Esophagus oesophagus
4 chr9:117531200-117532600 Enhancers Fetal Intestine Small intestine
5 chr9:117531400-117531800 Enhancers Gastric stomach
6 chr9:117531400-117532600 Enhancers Fetal Thymus thymus
7 chr9:117531400-117532800 Enhancers Fetal Lung lung
8 chr9:117531400-117533400 Enhancers Brain Germinal Matrix brain
9 chr9:117531600-117531800 Bivalent Enhancer Sigmoid Colon Sigmoid Colon
10 chr9:117531600-117532000 Enhancers Fetal Brain Male brain
11 chr9:117531600-117532000 Enhancers Fetal Kidney kidney
12 chr9:117531600-117532200 Enhancers Primary T helper 17 cells PMA-I stimulated --
13 chr9:117531600-117532600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr9:117531600-117532600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr9:117531600-117532600 Enhancers Osteobl bone
16 chr9:117531600-117532800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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