| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128656587-128657054 | Common:4; Rare:298; Clinvar (pathogenic):2 | ||||
| chr9:128683334-128683773 | Common:4; Rare:117 | ||||
| chr9:128684054-128684290 | Common:2; Rare:54 | ||||
| chr9:128684385-128684808 | Rare:115 | ||||
| chr9:128684878-128685260 | Rare:114 | ||||
| chr9:128688894-128689473 | Common:1; Rare:371 | ||||
| chr9:128689480-128689646 | Rare:101 | ||||
| chr9:128689747-128690147 | Rare:180 | ||||
| chr9:128702482-128702922 | Rare:140 | ||||
| chr9:128702980-128703590 | Common:3; Rare:154 | ||||
| chr9:128724040-128724477 | Common:6; Rare:305 | ||||
| chr9:128771806-128772065 | Common:4; Rare:151 | ||||
| chr9:128787070-128787367 | Common:7; Rare:168 | ||||
| chr9:128818267-128818714 | Common:7; Rare:209 | ||||
| chr9:128818774-128819230 | Common:2; Rare:180 |