Variant report
| Variant | rs58156462 |
|---|---|
| Chromosome Location | chr9:100555783-100555784 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:100554200-100556200 | Enhancers | Fetal Intestine Large | intestine |
| 2 | chr9:100554200-100557200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 3 | chr9:100554400-100563600 | Weak transcription | HMEC | breast |
| 4 | chr9:100554600-100555800 | Enhancers | K562 | blood |
| 5 | chr9:100554600-100557400 | Enhancers | Placenta | Placenta |
| 6 | chr9:100554800-100556000 | Enhancers | Fetal Intestine Small | intestine |
| 7 | chr9:100555000-100557400 | Enhancers | Placenta Amnion | Placenta Amnion |
| 8 | chr9:100555400-100555800 | Enhancers | NHEK | skin |
| 9 | chr9:100555600-100556000 | Enhancers | HepG2 | liver |
