| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97633517-97633872 | Common:4; Rare:115 | ||||
| chr9:97666573-97666805 | Common:1; Rare:37 | ||||
| chr9:97697249-97697516 | Common:2; Rare:140; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr9:97922456-97922580 | Common:3; Rare:65 | ||||
| chr9:97983129-97983448 | Common:1; Rare:121 | ||||
| chr9:97984460-97984553 | Rare:39 | ||||
| chr9:99221906-99222365 | Common:2; Rare:182; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:99906574-99906711 | Rare:66 | ||||
| chr9:100098966-100099329 | Common:3; Rare:104; Clinvar:2 | ||||
| chr9:100352803-100353089 | Rare:100 | ||||
| chr9:101028612-101028829 | Common:2; Rare:72 | ||||
| chr9:101398502-101398887 | Common:1; Rare:141 | ||||
| chr9:101435696-101435945 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:101533700-101533914 | Rare:65 | ||||
| chr9:104094431-104094604 | Common:2; Rare:47 |