| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125707146-125707375 | Common:2; Rare:77 | ||||
| chr9:125747338-125747649 | Common:1; Rare:114 | ||||
| chr9:125748927-125748954 | Rare:2 | ||||
| chr9:126804924-126805095 | Common:3; Rare:61 | ||||
| chr9:126860565-126860718 | Common:2; Rare:52 | ||||
| chr9:127245225-127245341 | Rare:22 | ||||
| chr9:127264744-127264907 | Rare:36 | ||||
| chr9:127424270-127424482 | Common:1; Rare:69 | ||||
| chr9:127451272-127451571 | Common:3; Rare:121; Clinvar (benign):1 | ||||
| chr9:127612001-127612394 | Common:2; Rare:142; Clinvar:4; Clinvar (benign):3 | ||||
| chr9:127735254-127735593 | Common:1; Rare:86 | ||||
| chr9:127755137-127755445 | Common:1; Rare:74 | ||||
| chr9:127802719-127803032 | Common:3; Rare:86 | ||||
| chr9:127877645-127877767 | Rare:29 | ||||
| chr9:127930774-127930934 | Common:2; Rare:41 |