| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:44761537-44761809 | Common:3; Rare:114 | ||||
| chr3:44861836-44861925 | Common:2; Rare:43 | ||||
| chr3:44974988-44975265 | Common:3; Rare:37 | ||||
| chr3:44975383-44975463 | Common:1; Rare:19 | ||||
| chr3:44976018-44976280 | Common:4; Rare:97 | ||||
| chr3:45146299-45146504 | Common:1; Rare:72 | ||||
| chr3:45689180-45689464 | Common:1; Rare:96 | ||||
| chr3:45796358-45796687 | Common:3; Rare:115; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:45842089-45842157 | Rare:17 | ||||
| chr3:45943229-45943469 | Rare:43 | ||||
| chr3:46407037-46407275 | Rare:43 | ||||
| chr3:46693642-46693770 | Common:1; Rare:34 | ||||
| chr3:46979508-46979857 | Common:3; Rare:88; Clinvar:2 | ||||
| chr3:46981981-46982185 | Rare:32 | ||||
| chr3:47163921-47164260 | Common:1; Rare:97 |