| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128103171-128103362 | Common:1; Rare:42 | ||||
| chr9:128191484-128191638 | Rare:49 | ||||
| chr9:128191750-128191848 | Common:1; Rare:25 | ||||
| chr9:128275925-128276307 | Common:5; Rare:172 | ||||
| chr9:128322410-128322621 | Common:1; Rare:61 | ||||
| chr9:128322751-128322870 | Common:2; Rare:49; Clinvar (benign):5 | ||||
| chr9:128371058-128371414 | Common:2; Rare:113 | ||||
| chr9:128552408-128552611 | Rare:79; Clinvar:1 | ||||
| chr9:128689450-128689643 | Rare:71 | ||||
| chr9:128724069-128724472 | Common:3; Rare:136 | ||||
| chr9:128771854-128772024 | Rare:43 | ||||
| chr9:128787149-128787333 | Common:3; Rare:61 | ||||
| chr9:128881929-128882235 | Common:2; Rare:108 | ||||
| chr9:128921976-128922331 | Common:1; Rare:79 | ||||
| chr9:128947580-128947722 | Common:1; Rare:59; Clinvar:3; Clinvar (benign):1 |