| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:93451477-93451886 | Common:3; Rare:120 | ||||
| chr9:94030716-94030877 | Common:1; Rare:55 | ||||
| chr9:95875969-95876033 | Common:4; Rare:31 | ||||
| chr9:96383654-96383786 | Common:1; Rare:45 | ||||
| chr9:96566818-96567020 | Common:1; Rare:55 | ||||
| chr9:97633347-97633829 | Common:6; Rare:149 | ||||
| chr9:99221906-99222329 | Common:2; Rare:160; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:100098923-100099255 | Common:2; Rare:92 | ||||
| chr9:100352895-100353060 | Rare:48 | ||||
| chr9:101398597-101398898 | Common:1; Rare:97 | ||||
| chr9:108933940-108933976 | Common:1; Rare:14; Clinvar:3 | ||||
| chr9:108934055-108934421 | Common:7; Rare:129; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:111631181-111631387 | Common:1; Rare:58 | ||||
| chr9:112379863-112380138 | Common:1; Rare:116 | ||||
| chr9:113221242-113221596 | Common:1; Rare:114 |