| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33473881-33474131 | Common:2; Rare:72 | ||||
| chr9:34126371-34126445 | Rare:28 | ||||
| chr9:34329228-34329594 | Rare:110 | ||||
| chr9:34637732-34638125 | Common:3; Rare:103 | ||||
| chr9:35111518-35111848 | Common:1; Rare:84 | ||||
| chr9:35658004-35658354 | Common:6; Rare:256; Clinvar:18; Clinvar (benign):10; Clinvar (pathogenic):33 | ||||
| chr9:35689705-35690057 | Common:3; Rare:117; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35732078-35732718 | Common:5; Rare:176 | ||||
| chr9:35748910-35749322 | Common:3; Rare:131 | ||||
| chr9:35815012-35815247 | Rare:58 | ||||
| chr9:35906600-35906765 | Common:7; Rare:64 | ||||
| chr9:36191158-36191268 | Rare:26 | ||||
| chr9:37800702-37800847 | Rare:45 | ||||
| chr9:37903992-37904198 | Rare:63 | ||||
| chr9:70258860-70259057 | Common:2; Rare:93 |