| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128340423-128340712 | Common:2; Rare:91 | ||||
| chr9:128371128-128371432 | Common:1; Rare:107 | ||||
| chr9:128455802-128456203 | Common:2; Rare:125 | ||||
| chr9:128504598-128504806 | Rare:98; Clinvar:5 | ||||
| chr9:128552388-128552648 | Rare:101; Clinvar:5 | ||||
| chr9:128566961-128566991 | Rare:8; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:128656652-128657129 | Common:2; Rare:151; Clinvar (pathogenic):1 | ||||
| chr9:128689422-128689643 | Rare:76 | ||||
| chr9:128771860-128772051 | Common:1; Rare:55 | ||||
| chr9:128787155-128787365 | Common:3; Rare:71 | ||||
| chr9:128881888-128882197 | Common:2; Rare:97 | ||||
| chr9:128882537-128882660 | Common:1; Rare:23 | ||||
| chr9:128947537-128947732 | Common:1; Rare:88; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:129036335-129036680 | Common:3; Rare:92 | ||||
| chr9:129080728-129081053 | Common:2; Rare:75 |