| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42600905-42601000 | Rare:38 | ||||
| chr3:42773223-42773332 | Common:1; Rare:29 | ||||
| chr3:42804427-42804635 | Common:2; Rare:61 | ||||
| chr3:43286434-43286654 | Common:2; Rare:97 | ||||
| chr3:43690817-43690998 | Common:3; Rare:99; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338720-44338807 | Common:2; Rare:30 | ||||
| chr3:44584618-44584916 | Rare:59 | ||||
| chr3:44729552-44729667 | Common:1; Rare:44 | ||||
| chr3:44761590-44761829 | Common:3; Rare:86 | ||||
| chr3:44861781-44861927 | Common:2; Rare:66 | ||||
| chr3:44976095-44976279 | Common:2; Rare:75 | ||||
| chr3:45689180-45689464 | Common:1; Rare:96 | ||||
| chr3:45842071-45842295 | Common:1; Rare:62 | ||||
| chr3:45995809-45995961 | Common:2; Rare:33; Clinvar:1 | ||||
| chr3:46407037-46407288 | Rare:46 |