| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97501506-97501798 | Common:6; Rare:75 | ||||
| chr9:97633275-97633488 | Common:2; Rare:60 | ||||
| chr9:97633497-97633915 | Common:5; Rare:131 | ||||
| chr9:97922154-97922320 | Common:1; Rare:61 | ||||
| chr9:97922417-97922574 | Common:4; Rare:82 | ||||
| chr9:97984515-97984589 | Common:1; Rare:37 | ||||
| chr9:98119188-98119322 | Common:1; Rare:33 | ||||
| chr9:98255576-98255830 | Common:3; Rare:75 | ||||
| chr9:98943187-98943590 | Common:1; Rare:72 | ||||
| chr9:98943779-98944049 | Common:3; Rare:94 | ||||
| chr9:99221605-99221666 | Rare:27; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:99221892-99222365 | Common:2; Rare:191; Clinvar:4; Clinvar (benign):3 | ||||
| chr9:99821610-99822036 | Rare:122 | ||||
| chr9:99906563-99906717 | Rare:69 | ||||
| chr9:100098958-100099350 | Common:4; Rare:113; Clinvar:2; Clinvar (benign):1 |