| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:58491830-58492138 | Common:3; Rare:83 | ||||
| chr3:58537161-58537355 | Common:2; Rare:39 | ||||
| chr3:61251400-61251594 | Common:4; Rare:51 | ||||
| chr3:62318888-62319049 | Rare:69 | ||||
| chr3:63863777-63864103 | Common:7; Rare:108 | ||||
| chr3:67654567-67654795 | Common:2; Rare:87 | ||||
| chr3:69013588-69013756 | Rare:45 | ||||
| chr3:69739249-69739557 | Rare:98 | ||||
| chr3:72996912-72997030 | Rare:42 | ||||
| chr3:87227032-87227386 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058946-88059325 | Common:2; Rare:143 | ||||
| chr3:88149613-88150033 | Common:3; Rare:117 | ||||
| chr3:93979947-93980190 | Common:3; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:94062904-94063059 | Rare:41 | ||||
| chr3:97764623-97764795 | Common:1; Rare:40; Clinvar (benign):1 |