| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97633288-97633453 | Rare:43 | ||||
| chr9:97633528-97633851 | Common:4; Rare:102 | ||||
| chr9:97922171-97922327 | Common:1; Rare:56 | ||||
| chr9:97922471-97922580 | Common:3; Rare:55 | ||||
| chr9:97983112-97983448 | Common:1; Rare:128 | ||||
| chr9:97984481-97984586 | Common:1; Rare:54 | ||||
| chr9:98056510-98056783 | Common:1; Rare:90 | ||||
| chr9:98374623-98374830 | Common:5; Rare:45 | ||||
| chr9:99221906-99222355 | Common:2; Rare:175; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:99906597-99906711 | Rare:54 | ||||
| chr9:100098966-100099314 | Common:3; Rare:99; Clinvar:2 | ||||
| chr9:100352858-100353081 | Rare:80 | ||||
| chr9:100427120-100427384 | Common:3; Rare:95 | ||||
| chr9:101398544-101398910 | Common:1; Rare:132 | ||||
| chr9:101487050-101487248 | Common:3; Rare:53 |