| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125241176-125241675 | Common:3; Rare:147 | ||||
| chr9:125261708-125261916 | Common:2; Rare:73 | ||||
| chr9:125706978-125707063 | Rare:16 | ||||
| chr9:125748921-125748953 | Rare:2 | ||||
| chr9:127122716-127122933 | Common:3; Rare:55 | ||||
| chr9:127245188-127245352 | Common:1; Rare:40 | ||||
| chr9:127424300-127424450 | Common:1; Rare:46 | ||||
| chr9:127451365-127451571 | Common:3; Rare:68; Clinvar (benign):1 | ||||
| chr9:127578960-127579315 | Common:7; Rare:74 | ||||
| chr9:127611984-127612439 | Common:2; Rare:161; Clinvar:5; Clinvar (benign):5 | ||||
| chr9:127877634-127877847 | Rare:59 | ||||
| chr9:127916927-127917277 | Common:1; Rare:98 | ||||
| chr9:128091319-128091484 | Rare:33 | ||||
| chr9:128128369-128128548 | Common:2; Rare:90 | ||||
| chr9:128191431-128191678 | Rare:71 |