| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:58433787-58433923 | Rare:57; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:61251383-61251594 | Common:4; Rare:53 | ||||
| chr3:61561412-61561656 | Common:2; Rare:86 | ||||
| chr3:62318927-62319055 | Rare:51 | ||||
| chr3:63863779-63864110 | Common:7; Rare:111 | ||||
| chr3:67654562-67654770 | Common:2; Rare:83 | ||||
| chr3:69013179-69013334 | Rare:41 | ||||
| chr3:69013579-69013819 | Common:1; Rare:73 | ||||
| chr3:69542514-69542754 | Common:3; Rare:65 | ||||
| chr3:69739224-69739535 | Rare:99 | ||||
| chr3:73624132-73624477 | Common:6; Rare:105 | ||||
| chr3:73625261-73625286 | Rare:6 | ||||
| chr3:81761420-81761828 | Common:8; Rare:146; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:87227220-87227512 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:88058917-88059304 | Common:3; Rare:146 |