Variant report
| Variant | rs16907148 |
|---|---|
| Chromosome Location | chr9:93852835-93852836 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:93847800-93855600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr9:93851600-93853200 | Enhancers | HepG2 | liver |
| 3 | chr9:93851800-93853000 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
| 4 | chr9:93851800-93853200 | Enhancers | IMR90 fetal lung fibroblasts Cell Line | lung |
| 5 | chr9:93852000-93853200 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 6 | chr9:93852400-93853200 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 7 | chr9:93852400-93853200 | Enhancers | Lung | lung |
| 8 | chr9:93852600-93853600 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
| 9 | chr9:93852600-93853800 | Weak transcription | Skeletal Muscle Female | skeletal muscle |
| 10 | chr9:93852600-93855400 | Weak transcription | Fetal Intestine Small | intestine |
| 11 | chr9:93852600-93859800 | Weak transcription | Fetal Heart | heart |
| 12 | chr9:93852600-93861600 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 13 | chr9:93852800-93861200 | Weak transcription | NHLF | lung |
