Variant report

Variant rs960957
Chromosome Location chr9:116533020-116533021
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116530600-116533600 Weak transcription Aorta Aorta
2 chr9:116530800-116534600 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr9:116531800-116535400 Enhancers Fetal Stomach stomach
4 chr9:116532000-116536000 Enhancers Fetal Muscle Leg muscle
5 chr9:116532200-116534800 Enhancers Fetal Muscle Trunk muscle
6 chr9:116532600-116534200 Enhancers Left Ventricle heart
7 chr9:116532800-116533600 Bivalent Enhancer Muscle Satellite Cultured Cells --
8 chr9:116532800-116533800 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:116532800-116533800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
10 chr9:116532800-116534000 Enhancers Lung lung
11 chr9:116532800-116534200 Enhancers Skeletal Muscle Male skeletal muscle
12 chr9:116532800-116534600 Bivalent Enhancer Fetal Lung lung
13 chr9:116532800-116534800 Enhancers HSMMtube muscle
14 chr9:116532800-116535000 Enhancers Ovary ovary
15 chr9:116532800-116535200 Enhancers Adipose Nuclei Adipose
16 chr9:116532800-116535400 Bivalent Enhancer NHDF-Ad bronchial
17 chr9:116533000-116534200 Enhancers Fetal Heart heart
18 chr9:116533000-116534200 Enhancers Skeletal Muscle Female skeletal muscle

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