| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:45378669-45378767 | Rare:21; Clinvar:1 | ||||
| chr15:45402143-45402523 | Common:6; Rare:126; Clinvar:1 | ||||
| chr15:45522732-45522925 | Common:1; Rare:63 | ||||
| chr15:45587008-45587488 | Common:2; Rare:122; Clinvar:6; Clinvar (benign):2 | ||||
| chr15:45587533-45587732 | Common:1; Rare:70; Clinvar (benign):1 | ||||
| chr15:45634701-45635310 | Common:2; Rare:156 | ||||
| chr15:48177503-48177726 | Rare:39 | ||||
| chr15:48177860-48177909 | Rare:13 | ||||
| chr15:48178133-48178484 | Common:1; Rare:101 | ||||
| chr15:48178504-48178519 | Rare:1 | ||||
| chr15:48331005-48331168 | Common:3; Rare:42 | ||||
| chr15:48331285-48331670 | Common:5; Rare:139 | ||||
| chr15:48331741-48332330 | Common:9; Rare:192; Clinvar:1 | ||||
| chr15:48645394-48645482 | Rare:30 | ||||
| chr15:48645634-48645903 | Common:2; Rare:82; Clinvar (benign):1 |