| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42581895-42582137 | Common:3; Rare:76 | ||||
| chr3:42600372-42600741 | Common:2; Rare:146 | ||||
| chr3:42701486-42701654 | Common:1; Rare:27 | ||||
| chr3:42702580-42702927 | Rare:77 | ||||
| chr3:42804422-42804663 | Common:2; Rare:71 | ||||
| chr3:44338387-44338463 | Rare:26 | ||||
| chr3:44624913-44625063 | Common:2; Rare:41 | ||||
| chr3:44761577-44761768 | Common:3; Rare:78 | ||||
| chr3:44861767-44861927 | Common:2; Rare:72 | ||||
| chr3:44976080-44976287 | Common:2; Rare:85 | ||||
| chr3:45689169-45689459 | Common:2; Rare:96 | ||||
| chr3:45842061-45842254 | Common:1; Rare:48 | ||||
| chr3:45995739-45995981 | Common:3; Rare:52; Clinvar:1 | ||||
| chr3:46693642-46693817 | Common:1; Rare:41 | ||||
| chr3:46863260-46863697 | Common:3; Rare:107; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):1 |