| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69013658-69013750 | Rare:22 | ||||
| chr3:69052219-69052413 | Common:3; Rare:74 | ||||
| chr3:88058946-88059255 | Common:2; Rare:98 | ||||
| chr3:88149864-88149993 | Rare:42 | ||||
| chr3:94062910-94063040 | Rare:35 | ||||
| chr3:97764454-97764774 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr3:98522601-98522755 | Rare:35 | ||||
| chr3:99817537-99817946 | Common:1; Rare:132 | ||||
| chr3:99876124-99876254 | Rare:33 | ||||
| chr3:100260713-100261039 | Rare:90 | ||||
| chr3:100401398-100401580 | Common:1; Rare:34 | ||||
| chr3:100492393-100492642 | Common:2; Rare:87 | ||||
| chr3:100709224-100709393 | Common:2; Rare:63 | ||||
| chr3:101561777-101561910 | Common:1; Rare:42 | ||||
| chr3:101574049-101574225 | Rare:57 |