| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97411760-97412170 | Common:7; Rare:184; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:97501506-97501712 | Common:6; Rare:56 | ||||
| chr9:97633020-97633864 | Common:12; Rare:494 | ||||
| chr9:97697293-97697493 | Common:3; Rare:181; Clinvar:10; Clinvar (benign):2 | ||||
| chr9:97922174-97922320 | Common:2; Rare:83 | ||||
| chr9:97922445-97922628 | Common:8; Rare:170 | ||||
| chr9:97982990-97983497 | Common:3; Rare:364 | ||||
| chr9:97984100-97984500 | Common:2; Rare:270 | ||||
| chr9:97984659-97984915 | Common:6; Rare:245 | ||||
| chr9:98056528-98056791 | Common:4; Rare:183 | ||||
| chr9:98118720-98119120 | Common:1; Rare:172 | ||||
| chr9:98192608-98192859 | Common:11; Rare:127 | ||||
| chr9:98255320-98255871 | Common:8; Rare:266 | ||||
| chr9:98256069-98256179 | Rare:25 | ||||
| chr9:99104783-99105187 | Common:4; Rare:265; Clinvar (benign):2 |