| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127424236-127424488 | Common:2; Rare:119 | ||||
| chr9:127450990-127451310 | Common:6; Rare:188 | ||||
| chr9:127451364-127451626 | Common:3; Rare:74; Clinvar (benign):1 | ||||
| chr9:127568944-127569338 | Common:9; Rare:135 | ||||
| chr9:127578830-127579300 | Common:14; Rare:185 | ||||
| chr9:127612001-127612288 | Common:2; Rare:216; Clinvar:5; Clinvar (benign):2 | ||||
| chr9:127785942-127786173 | Common:2; Rare:168; Clinvar:1 | ||||
| chr9:127786208-127786930 | Common:5; Rare:351 | ||||
| chr9:127802567-127803032 | Common:5; Rare:168 | ||||
| chr9:127877654-127877773 | Rare:38 | ||||
| chr9:127897280-127897570 | Common:2; Rare:119 | ||||
| chr9:127899498-127899712 | Rare:75 | ||||
| chr9:127916965-127917319 | Common:1; Rare:107 | ||||
| chr9:127937803-127937977 | Common:3; Rare:81; Clinvar:7; Clinvar (benign):4 | ||||
| chr9:127950578-127950873 | Rare:64 |