| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:96566778-96566946 | Common:2; Rare:99 | ||||
| chr9:96618421-96618830 | Common:4; Rare:245 | ||||
| chr9:96619754-96620188 | Common:1; Rare:163 | ||||
| chr9:96655190-96655392 | Common:2; Rare:119 | ||||
| chr9:96778049-96778156 | Rare:34 | ||||
| chr9:96854287-96854549 | Common:4; Rare:72 | ||||
| chr9:96854468-96854673 | Common:3; Rare:46 | ||||
| chr9:97013571-97013843 | Common:8; Rare:141 | ||||
| chr9:97412001-97412221 | Common:6; Rare:94; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:97633271-97633878 | Common:11; Rare:345 | ||||
| chr9:97697280-97697516 | Common:3; Rare:196; Clinvar:10; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr9:97922456-97922619 | Common:8; Rare:155 | ||||
| chr9:97983021-97983458 | Common:2; Rare:323 | ||||
| chr9:97983615-97984496 | Common:12; Rare:768 | ||||
| chr9:98056437-98056853 | Common:6; Rare:241 |