Variant report

Variant rs56373906
Chromosome Location chr9:92747099-92747100
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:92745000-92752800 Weak transcription Liver Liver
2 chr9:92745000-92755400 Weak transcription Psoas Muscle Psoas
3 chr9:92745400-92747600 Enhancers NHEK skin
4 chr9:92745400-92747800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr9:92745400-92748600 Enhancers HMEC breast
6 chr9:92745800-92747800 Enhancers Osteobl bone
7 chr9:92746000-92747800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr9:92746000-92747800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr9:92746000-92747800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr9:92746000-92747800 Enhancers HSMM muscle
11 chr9:92746000-92747800 Enhancers HSMMtube muscle
12 chr9:92746400-92747200 Enhancers Muscle Satellite Cultured Cells --
13 chr9:92746400-92748000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr9:92746600-92747800 Enhancers NHLF lung
15 chr9:92746800-92747600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr9:92746800-92747600 Enhancers NHDF-Ad bronchial
17 chr9:92746800-92748200 Enhancers GM12878-XiMat blood

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