| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:145052198-145052504 | Common:10; Rare:87 | ||||
| chr9:178912-179215 | Common:7; Rare:67 | ||||
| chr9:470139-470343 | Common:16; Rare:86 | ||||
| chr9:706778-707171 | Common:3; Rare:129 | ||||
| chr9:2015066-2015393 | Common:3; Rare:94 | ||||
| chr9:2017476-2017699 | Rare:66 | ||||
| chr9:2158355-2158587 | Rare:56 | ||||
| chr9:2621526-2621799 | Common:2; Rare:113; Clinvar:1 | ||||
| chr9:2621996-2622156 | Common:4; Rare:53; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:2622226-2622273 | Rare:21; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:2844034-2844368 | Common:6; Rare:133 | ||||
| chr9:3525871-3526119 | Common:1; Rare:110 | ||||
| chr9:3526409-3526518 | Common:4; Rare:59 | ||||
| chr9:4662268-4662323 | Common:1; Rare:18 | ||||
| chr9:4679423-4679721 | Common:1; Rare:130 |