| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133375929-133376340 | Common:3; Rare:143 | ||||
| chr9:133417908-133418101 | Common:2; Rare:52 | ||||
| chr9:134135358-134135424 | Common:1; Rare:12 | ||||
| chr9:135499848-135499966 | Common:3; Rare:34 | ||||
| chr9:136118736-136119039 | Common:5; Rare:112 | ||||
| chr9:136410603-136410678 | Rare:38 | ||||
| chr9:136546193-136546233 | Rare:15 | ||||
| chr9:136662659-136662996 | Common:1; Rare:79 | ||||
| chr9:136687360-136687658 | Common:2; Rare:87; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:136745813-136746176 | Common:1; Rare:105 | ||||
| chr9:136746183-136746448 | Common:2; Rare:40 | ||||
| chr9:136849587-136849765 | Common:1; Rare:68 | ||||
| chr9:136944592-136944839 | Rare:105 | ||||
| chr9:136977430-136977580 | Rare:33 | ||||
| chr9:137086631-137087146 | Common:2; Rare:213; Clinvar:6; Clinvar (benign):1 |