| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127122533-127123001 | Common:4; Rare:126 | ||||
| chr9:127224379-127224652 | Rare:74 | ||||
| chr9:127245188-127245341 | Common:1; Rare:37 | ||||
| chr9:127424081-127424440 | Common:1; Rare:104 | ||||
| chr9:127450735-127451062 | Common:3; Rare:73 | ||||
| chr9:127451274-127451565 | Common:3; Rare:120; Clinvar (benign):1 | ||||
| chr9:127802766-127803041 | Common:3; Rare:77 | ||||
| chr9:127899518-127899780 | Common:2; Rare:90 | ||||
| chr9:128091291-128091462 | Rare:35 | ||||
| chr9:128098289-128098537 | Common:1; Rare:52 | ||||
| chr9:128160034-128160399 | Common:2; Rare:87 | ||||
| chr9:128191494-128191642 | Rare:45 | ||||
| chr9:128191750-128191784 | Rare:10 | ||||
| chr9:128191789-128191867 | Rare:18 | ||||
| chr9:128204215-128204347 | Rare:32 |