| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:13420206-13420440 | Common:1; Rare:67 | ||||
| chr3:13479993-13480419 | Common:4; Rare:106 | ||||
| chr3:13548990-13549170 | Common:1; Rare:59 | ||||
| chr3:14124728-14125105 | Common:4; Rare:107; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178564-14178886 | Common:2; Rare:171; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402457-14402632 | Rare:45 | ||||
| chr3:14651486-14651833 | Rare:108 | ||||
| chr3:14947258-14947569 | Common:3; Rare:141 | ||||
| chr3:14948023-14948197 | Rare:80 | ||||
| chr3:14948413-14948637 | Common:2; Rare:63 | ||||
| chr3:15065233-15065399 | Common:2; Rare:59 | ||||
| chr3:15099119-15099283 | Rare:39 | ||||
| chr3:15205976-15206332 | Common:1; Rare:129 | ||||
| chr3:15427459-15427635 | Common:1; Rare:64 | ||||
| chr3:15601469-15602046 | Common:6; Rare:263; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):1 |