| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:71130539-71130674 | Rare:50; Clinvar:2 | ||||
| chr3:72996738-72997067 | Rare:123 | ||||
| chr3:81761516-81761735 | Common:8; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:81761738-81761800 | Rare:14 | ||||
| chr3:86991070-86991379 | Common:1; Rare:75 | ||||
| chr3:87227189-87227395 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058914-88059322 | Common:3; Rare:157 | ||||
| chr3:88149628-88150040 | Common:4; Rare:119 | ||||
| chr3:93979967-93980211 | Common:4; Rare:87; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94062897-94063069 | Rare:44 | ||||
| chr3:97764461-97764795 | Common:1; Rare:76; Clinvar (benign):1 | ||||
| chr3:98522601-98522690 | Rare:23 | ||||
| chr3:98732442-98732512 | Rare:13 | ||||
| chr3:98732696-98732734 | Rare:8 | ||||
| chr3:99638529-99638666 | Rare:31 |