| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:124291680-124292019 | Common:4; Rare:70 | ||||
| chr9:124861878-124862160 | Common:1; Rare:127 | ||||
| chr9:124862325-124862370 | Rare:9 | ||||
| chr9:124940946-124941152 | Common:3; Rare:71 | ||||
| chr9:125189603-125190046 | Common:1; Rare:188 | ||||
| chr9:125200402-125200596 | Common:1; Rare:78 | ||||
| chr9:125240658-125241131 | Rare:121 | ||||
| chr9:125241230-125241686 | Common:3; Rare:134 | ||||
| chr9:125650421-125650480 | Rare:7 | ||||
| chr9:126804880-126805113 | Common:3; Rare:81 | ||||
| chr9:126860602-126860718 | Common:1; Rare:40 | ||||
| chr9:127122595-127122918 | Common:4; Rare:80 | ||||
| chr9:127424317-127424499 | Common:1; Rare:57 | ||||
| chr9:127451365-127451567 | Common:3; Rare:68; Clinvar (benign):1 | ||||
| chr9:127578986-127579339 | Common:4; Rare:66 |