| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127877645-127877751 | Rare:28 | ||||
| chr9:127897315-127897523 | Common:1; Rare:47 | ||||
| chr9:127916982-127917243 | Common:1; Rare:75 | ||||
| chr9:127937824-127937932 | Common:1; Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:127980990-127981226 | Common:2; Rare:72 | ||||
| chr9:128067308-128067646 | Common:3; Rare:72 | ||||
| chr9:128098289-128098537 | Common:1; Rare:52 | ||||
| chr9:128127557-128127813 | Common:3; Rare:82 | ||||
| chr9:128128433-128128482 | Rare:19 | ||||
| chr9:128160113-128160455 | Common:2; Rare:89 | ||||
| chr9:128167138-128167313 | Rare:36 | ||||
| chr9:128169136-128169522 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:128191388-128191668 | Rare:81 | ||||
| chr9:128191750-128191933 | Common:1; Rare:50 | ||||
| chr9:128203254-128203416 | Common:1; Rare:60 |