| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:72996634-72997030 | Common:3; Rare:165 | ||||
| chr3:77039917-77040119 | Common:3; Rare:63 | ||||
| chr3:87227032-87227414 | Common:2; Rare:110; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058946-88059261 | Common:2; Rare:101 | ||||
| chr3:88149605-88149686 | Common:1; Rare:21 | ||||
| chr3:88149862-88150049 | Common:5; Rare:77 | ||||
| chr3:93979947-93980201 | Common:4; Rare:91; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:97764448-97764795 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr3:97821868-97822024 | Rare:51 | ||||
| chr3:98522858-98523140 | Common:1; Rare:82 | ||||
| chr3:98901672-98901984 | Common:1; Rare:112 | ||||
| chr3:99817555-99817912 | Rare:104 | ||||
| chr3:100260743-100261021 | Rare:71 | ||||
| chr3:100334628-100334780 | Common:1; Rare:65 | ||||
| chr3:100401402-100401602 | Common:1; Rare:36 |