| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35732373-35732683 | Common:3; Rare:78 | ||||
| chr9:35748989-35749342 | Common:2; Rare:131 | ||||
| chr9:36136621-36136775 | Common:2; Rare:51 | ||||
| chr9:36190715-36190967 | Common:1; Rare:86 | ||||
| chr9:36258380-36258622 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37120208-37120614 | Common:2; Rare:129 | ||||
| chr9:37485729-37486000 | Common:1; Rare:96 | ||||
| chr9:37785024-37785149 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:37800707-37800794 | Rare:25 | ||||
| chr9:37904084-37904222 | Rare:43 | ||||
| chr9:68356354-68356659 | Common:7; Rare:57 | ||||
| chr9:68779950-68780070 | Common:1; Rare:36 | ||||
| chr9:69759904-69760107 | Common:2; Rare:91 | ||||
| chr9:70043911-70043951 | Rare:7 | ||||
| chr9:70044052-70044130 | Rare:19 |