| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:27573430-27573524 | Common:5; Rare:50 | ||||
| chr9:27573732-27573972 | Common:2; Rare:76; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:32384491-32384732 | Common:1; Rare:91 | ||||
| chr9:33025083-33025383 | Common:7; Rare:124 | ||||
| chr9:33166760-33166966 | Rare:66; Clinvar:3 | ||||
| chr9:33167083-33167530 | Common:1; Rare:159; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:33264736-33265094 | Rare:93 | ||||
| chr9:33290394-33290571 | Common:2; Rare:68 | ||||
| chr9:33401353-33401687 | Common:3; Rare:65 | ||||
| chr9:33402453-33402778 | Rare:62 | ||||
| chr9:33473841-33474144 | Common:4; Rare:94 | ||||
| chr9:33817531-33817934 | Common:2; Rare:111 | ||||
| chr9:34048870-34048992 | Common:1; Rare:49 | ||||
| chr9:34329292-34329614 | Common:1; Rare:89 | ||||
| chr9:34458551-34458794 | Rare:60 |