| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57227597-57227922 | Common:4; Rare:109 | ||||
| chr3:57556006-57556298 | Rare:67 | ||||
| chr3:57597330-57597768 | Common:4; Rare:127 | ||||
| chr3:61561412-61561656 | Common:2; Rare:86 | ||||
| chr3:62318932-62319046 | Rare:44 | ||||
| chr3:67654582-67654761 | Common:2; Rare:68 | ||||
| chr3:69013648-69013790 | Common:1; Rare:42 | ||||
| chr3:69052204-69052466 | Common:6; Rare:91 | ||||
| chr3:72996651-72997030 | Common:3; Rare:154 | ||||
| chr3:81761502-81761841 | Common:8; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:87227210-87227371 | Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:88058935-88059323 | Common:2; Rare:148 | ||||
| chr3:93979935-93980190 | Common:3; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:94062910-94063060 | Rare:38 | ||||
| chr3:97764504-97764802 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 |