Variant report
| Variant | rs58659483 |
|---|---|
| Chromosome Location | chr9:116544452-116544453 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:116539000-116551400 | Weak transcription | Fetal Kidney | kidney |
| 2 | chr9:116543200-116550200 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
| 3 | chr9:116543800-116547200 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 4 | chr9:116544000-116544600 | Enhancers | Primary monocytes fromperipheralblood | blood |
| 5 | chr9:116544000-116544800 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 6 | chr9:116544200-116544600 | Enhancers | Monocytes-CD14+_RO01746 | blood |
| 7 | chr9:116544400-116544600 | Bivalent Enhancer | H1 Derived Mesenchymal Stem Cells | ES cell derived |
