| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128504598-128504849 | Rare:111; Clinvar:6 | ||||
| chr9:128552394-128552622 | Rare:88; Clinvar:1 | ||||
| chr9:128656635-128657067 | Common:2; Rare:136; Clinvar (pathogenic):1 | ||||
| chr9:128683634-128684003 | Rare:102 | ||||
| chr9:128684953-128685091 | Rare:25 | ||||
| chr9:128689422-128689643 | Rare:76 | ||||
| chr9:128724081-128724475 | Common:3; Rare:129 | ||||
| chr9:128771877-128771990 | Rare:30 | ||||
| chr9:128772456-128772487 | Rare:2 | ||||
| chr9:128787148-128787353 | Common:3; Rare:69 | ||||
| chr9:128881929-128882202 | Common:2; Rare:93 | ||||
| chr9:128947549-128947747 | Common:2; Rare:97; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:129036374-129036669 | Common:2; Rare:83 | ||||
| chr9:129110702-129110953 | Common:3; Rare:50 | ||||
| chr9:129111316-129111593 | Common:2; Rare:74 |