| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57227615-57227911 | Common:3; Rare:101 | ||||
| chr3:57556006-57556307 | Rare:71 | ||||
| chr3:57597314-57597724 | Common:4; Rare:125 | ||||
| chr3:62318891-62319068 | Rare:72 | ||||
| chr3:63863777-63864114 | Common:7; Rare:112 | ||||
| chr3:66038764-66039012 | Common:2; Rare:86 | ||||
| chr3:67654557-67654717 | Common:1; Rare:64 | ||||
| chr3:71130557-71130685 | Rare:53; Clinvar:1 | ||||
| chr3:72996715-72997030 | Common:2; Rare:117 | ||||
| chr3:87227186-87227395 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058942-88059308 | Common:2; Rare:136 | ||||
| chr3:88149605-88149723 | Common:1; Rare:27 | ||||
| chr3:94062897-94063011 | Rare:36 | ||||
| chr3:97764706-97764793 | Common:1; Rare:17; Clinvar (benign):1 | ||||
| chr3:98732471-98732501 | Rare:8 |