Variant report

Variant rs2921772
Chromosome Location chr8:117902111-117902112
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:117900000-117902800 Weak transcription HMEC breast
2 chr8:117901200-117903600 Enhancers HepG2 liver
3 chr8:117901200-117903800 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr8:117901600-117902200 Enhancers Osteobl bone
5 chr8:117901600-117902400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr8:117901600-117902600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr8:117901800-117902200 Enhancers Fetal Stomach stomach
8 chr8:117901800-117902400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chr8:117901800-117903200 Enhancers NHLF lung
10 chr8:117902000-117902200 Enhancers Duodenum Smooth Muscle Duodenum
11 chr8:117902000-117902200 Enhancers Fetal Thymus thymus
12 chr8:117902000-117902400 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr8:117902000-117902400 Enhancers NHDF-Ad bronchial
14 chr8:117902000-117903200 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr8:117902000-117903400 Flanking Active TSS Dnd41 blood
16 chr8:117902000-117903800 Enhancers Ovary ovary
17 chr8:117902000-117903800 Flanking Active TSS Hela-S3 cervix
18 chr8:117902000-117904000 Enhancers Fetal Lung lung

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