| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:96449929-96450150 | Common:2; Rare:75 | ||||
| chr9:96566820-96567037 | Common:1; Rare:58 | ||||
| chr9:96618586-96618667 | Common:1; Rare:37 | ||||
| chr9:96619865-96620043 | Common:1; Rare:46 | ||||
| chr9:96655294-96655413 | Rare:30 | ||||
| chr9:96778033-96778163 | Rare:39 | ||||
| chr9:96854492-96854641 | Common:1; Rare:35 | ||||
| chr9:96928629-96928919 | Common:1; Rare:14 | ||||
| chr9:97013677-97013820 | Common:2; Rare:40 | ||||
| chr9:97039040-97039402 | Common:1; Rare:140 | ||||
| chr9:97307258-97307387 | Common:1; Rare:42 | ||||
| chr9:97307585-97307762 | Common:3; Rare:47 | ||||
| chr9:97362006-97362296 | Common:2; Rare:72 | ||||
| chr9:97411888-97412183 | Common:4; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:97633271-97633886 | Common:6; Rare:190 |