Variant report

Variant rs2960687
Chromosome Location chr10:117532672-117532673
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:117529200-117533400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr10:117531000-117534400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr10:117531200-117534400 Enhancers NHDF-Ad bronchial
4 chr10:117531200-117534600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr10:117531200-117534600 Enhancers HSMM muscle
6 chr10:117531200-117534800 Enhancers Muscle Satellite Cultured Cells --
7 chr10:117531600-117533800 Enhancers NHLF lung
8 chr10:117531800-117532800 Weak transcription NH-A brain
9 chr10:117532200-117533200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr10:117532200-117533800 Enhancers HSMMtube muscle
11 chr10:117532400-117532800 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr10:117532400-117532800 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr10:117532400-117532800 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr10:117532400-117532800 Enhancers NHEK skin
15 chr10:117532400-117532800 Flanking Active TSS Osteobl bone
16 chr10:117532400-117533600 Enhancers Fetal Adrenal Gland Adrenal Gland
17 chr10:117532600-117533200 Weak transcription Aorta Aorta

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