| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34178885-34179077 | Common:1; Rare:54 | ||||
| chr9:34329186-34329640 | Common:1; Rare:143 | ||||
| chr9:34665381-34665660 | Rare:91 | ||||
| chr9:34989435-34989790 | Common:2; Rare:94 | ||||
| chr9:35079984-35080153 | Common:3; Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:35161773-35162084 | Common:4; Rare:89 | ||||
| chr9:35657857-35657923 | Common:2; Rare:67; Clinvar:14; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr9:35657925-35658322 | Common:5; Rare:330; Clinvar:26; Clinvar (benign):13; Clinvar (pathogenic):36 | ||||
| chr9:35732082-35732334 | Common:2; Rare:70 | ||||
| chr9:35732373-35732709 | Common:3; Rare:84 | ||||
| chr9:35748507-35748708 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:35748993-35749369 | Common:2; Rare:141 | ||||
| chr9:35814976-35815293 | Rare:79 | ||||
| chr9:36036728-36036957 | Common:2; Rare:70 | ||||
| chr9:36190676-36191063 | Common:2; Rare:122 |