| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35673869-35674026 | Common:2; Rare:55 | ||||
| chr9:35732089-35732334 | Common:1; Rare:70 | ||||
| chr9:35732399-35732671 | Common:2; Rare:64 | ||||
| chr9:35748954-35749379 | Common:2; Rare:153 | ||||
| chr9:35814975-35815275 | Rare:75 | ||||
| chr9:36258409-36258580 | Common:2; Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37464970-37465060 | Common:1; Rare:29 | ||||
| chr9:37800707-37800794 | Rare:25 | ||||
| chr9:37904084-37904212 | Rare:42 | ||||
| chr9:68356534-68356628 | Common:1; Rare:13 | ||||
| chr9:69759925-69760099 | Common:2; Rare:85 | ||||
| chr9:70258824-70259069 | Common:4; Rare:117 | ||||
| chr9:70413950-70414203 | Rare:51 | ||||
| chr9:71768505-71768605 | Rare:23 | ||||
| chr9:71911222-71911508 | Common:3; Rare:85 |