Variant report
| Variant | rs12348862 |
|---|---|
| Chromosome Location | chr9:117531308-117531309 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:117525800-117533000 | Weak transcription | Aorta | Aorta |
| 2 | chr9:117529400-117532600 | Enhancers | Fetal Intestine Large | intestine |
| 3 | chr9:117529800-117533400 | Weak transcription | Esophagus | oesophagus |
| 4 | chr9:117531200-117532600 | Enhancers | Fetal Intestine Small | intestine |
