| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95875448-95875719 | Common:1; Rare:96 | ||||
| chr9:95875961-95876062 | Common:5; Rare:52; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96655284-96655466 | Rare:49 | ||||
| chr9:96778054-96778154 | Rare:32 | ||||
| chr9:97412007-97412196 | Common:3; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:97633271-97633875 | Common:6; Rare:189 | ||||
| chr9:97922471-97922580 | Common:3; Rare:55 | ||||
| chr9:97983146-97983459 | Common:1; Rare:118 | ||||
| chr9:97983465-97983607 | Common:1; Rare:53 | ||||
| chr9:97984502-97984600 | Common:1; Rare:49 | ||||
| chr9:98119175-98119274 | Common:1; Rare:28 | ||||
| chr9:98255559-98255985 | Common:3; Rare:119 | ||||
| chr9:98943526-98943654 | Common:1; Rare:29 | ||||
| chr9:98943672-98944072 | Common:4; Rare:133 | ||||
| chr9:99221898-99222355 | Common:2; Rare:181; Clinvar:2; Clinvar (benign):3 |