| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:45587093-45587254 | Rare:29 | ||||
| chr15:45587308-45587474 | Rare:50; Clinvar:5 | ||||
| chr15:45587753-45587796 | Rare:9 | ||||
| chr15:48331383-48331453 | Rare:22 | ||||
| chr15:48645698-48646021 | Common:2; Rare:100; Clinvar (benign):1 | ||||
| chr15:48878017-48878590 | Common:1; Rare:214 | ||||
| chr15:49046352-49046663 | Common:2; Rare:109 | ||||
| chr15:49155570-49155845 | Common:2; Rare:94 | ||||
| chr15:49620810-49621114 | Common:6; Rare:117 | ||||
| chr15:50354859-50354992 | Rare:19 | ||||
| chr15:50355106-50355513 | Common:3; Rare:164 | ||||
| chr15:50686723-50686905 | Common:4; Rare:79 | ||||
| chr15:50765576-50765784 | Common:2; Rare:72 | ||||
| chr15:50908629-50908754 | Common:1; Rare:50; Clinvar (benign):2 | ||||
| chr15:51971741-51971822 | Rare:41 |