| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:126804958-126805115 | Common:3; Rare:58 | ||||
| chr9:127424319-127424460 | Common:1; Rare:43 | ||||
| chr9:127451365-127451519 | Common:2; Rare:55 | ||||
| chr9:127579005-127579312 | Common:4; Rare:60 | ||||
| chr9:127877671-127877791 | Rare:22 | ||||
| chr9:127916982-127917315 | Common:1; Rare:98 | ||||
| chr9:128191522-128191660 | Rare:37 | ||||
| chr9:128191753-128191848 | Common:1; Rare:24 | ||||
| chr9:128265593-128265822 | Common:2; Rare:73 | ||||
| chr9:128275900-128276302 | Common:5; Rare:176 | ||||
| chr9:128322417-128322586 | Common:1; Rare:51 | ||||
| chr9:128371196-128371398 | Rare:75 | ||||
| chr9:128455966-128456195 | Common:1; Rare:77 | ||||
| chr9:128552395-128552614 | Rare:82; Clinvar:1 | ||||
| chr9:128608953-128609206 | Rare:62; Clinvar:3; Clinvar (benign):3 |