| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:130042400-130042630 | Common:1; Rare:26 | ||||
| chr8:132957355-132957595 | Rare:52 | ||||
| chr8:133058377-133058606 | Common:2; Rare:41 | ||||
| chr8:133072192-133072371 | Common:1; Rare:29 | ||||
| chr8:133127095-133127201 | Common:2; Rare:14 | ||||
| chr8:143281613-143281799 | Common:3; Rare:48 | ||||
| chr8:145002858-145002969 | Rare:29 | ||||
| chr9:569393-569531 | Common:1; Rare:44 | ||||
| chr9:2267532-2267834 | Common:1; Rare:75 | ||||
| chr9:2709871-2710087 | Common:1; Rare:44 | ||||
| chr9:3508435-3508627 | Common:4; Rare:45 | ||||
| chr9:5629633-5629845 | Common:1; Rare:55 | ||||
| chr9:32550860-32551156 | Common:1; Rare:120; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:37025712-37025817 | Rare:34 | ||||
| chr9:37026425-37026599 | Common:1; Rare:46 |