Variant report

Variant rs2383077
Chromosome Location chr9:18538756-18538757
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18533200-18541200 Strong transcription Osteobl bone
2 chr9:18533600-18538800 Strong transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr9:18535000-18542400 Weak transcription NHLF lung
4 chr9:18535000-18542600 Weak transcription Fetal Stomach stomach
5 chr9:18535800-18540200 Strong transcription Muscle Satellite Cultured Cells --
6 chr9:18535800-18541000 Strong transcription NHDF-Ad bronchial
7 chr9:18535800-18541200 Strong transcription NH-A brain
8 chr9:18536000-18542200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr9:18536000-18542200 Strong transcription HSMM muscle
10 chr9:18536200-18539000 Weak transcription Fetal Heart heart
11 chr9:18536200-18542800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr9:18536800-18542400 Strong transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr9:18538000-18543400 Weak transcription HSMMtube muscle
14 chr9:18538400-18542400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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