| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132878269-132878430 | Common:1; Rare:62 | ||||
| chr9:133030445-133030767 | Common:4; Rare:91 | ||||
| chr9:133336130-133336345 | Common:1; Rare:85 | ||||
| chr9:133347961-133348258 | Common:3; Rare:98 | ||||
| chr9:133356443-133356599 | Common:1; Rare:70; Clinvar (benign):2 | ||||
| chr9:133376007-133376366 | Common:1; Rare:131 | ||||
| chr9:133417953-133418086 | Common:1; Rare:33 | ||||
| chr9:136118678-136119050 | Common:5; Rare:136 | ||||
| chr9:136327141-136327611 | Common:4; Rare:153 | ||||
| chr9:136410357-136410695 | Common:7; Rare:147 | ||||
| chr9:136658206-136658518 | Common:2; Rare:48 | ||||
| chr9:136659283-136659479 | Common:1; Rare:48 | ||||
| chr9:136662676-136663036 | Common:2; Rare:83 | ||||
| chr9:136663336-136663424 | Rare:12 | ||||
| chr9:136665492-136665822 | Common:2; Rare:84 |