| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33290347-33290563 | Common:2; Rare:80 | ||||
| chr9:34048863-34049025 | Common:1; Rare:64 | ||||
| chr9:34049175-34049267 | Common:1; Rare:22 | ||||
| chr9:34126665-34126795 | Common:1; Rare:42 | ||||
| chr9:34329181-34329638 | Common:1; Rare:142 | ||||
| chr9:34612073-34612223 | Common:8; Rare:54 | ||||
| chr9:34652017-34652189 | Rare:41 | ||||
| chr9:34665417-34665655 | Rare:74 | ||||
| chr9:35103054-35103288 | Common:1; Rare:85 | ||||
| chr9:35489906-35490127 | Common:1; Rare:62 | ||||
| chr9:35646823-35646951 | Rare:26 | ||||
| chr9:35657970-35658326 | Common:5; Rare:279; Clinvar:20; Clinvar (benign):11; Clinvar (pathogenic):34 | ||||
| chr9:35689813-35690130 | Common:4; Rare:107; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35732089-35732649 | Common:3; Rare:160 | ||||
| chr9:35748999-35749342 | Common:2; Rare:129 |