| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33798900-33798926 | Rare:14 | ||||
| chr3:36992692-36992847 | Rare:58 | ||||
| chr3:36993034-36993546 | Common:2; Rare:172; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr3:36993663-36993835 | Rare:71; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:37176212-37176389 | Rare:56 | ||||
| chr3:37243150-37243378 | Common:1; Rare:59 | ||||
| chr3:38138576-38138701 | Common:2; Rare:50; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:39051917-39052055 | Common:1; Rare:48 | ||||
| chr3:39107390-39107741 | Common:5; Rare:102 | ||||
| chr3:39383289-39383433 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:39383570-39383647 | Rare:17 | ||||
| chr3:39406811-39407062 | Common:3; Rare:97 | ||||
| chr3:40309479-40309813 | Common:9; Rare:114 | ||||
| chr3:40457175-40457376 | Common:3; Rare:95 | ||||
| chr3:40477058-40477184 | Common:1; Rare:32 |