| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43330525-43330700 | Rare:63 | ||||
| chr15:43371021-43371110 | Rare:18 | ||||
| chr15:44288386-44288796 | Common:39; Rare:234 | ||||
| chr15:44711289-44711613 | Rare:95; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45587107-45587243 | Rare:21 | ||||
| chr15:45587300-45587591 | Rare:102; Clinvar:7; Clinvar (benign):2 | ||||
| chr15:48645667-48646015 | Common:2; Rare:107; Clinvar (benign):1 | ||||
| chr15:48878021-48878182 | Rare:60 | ||||
| chr15:49155558-49155819 | Common:2; Rare:87 | ||||
| chr15:49423111-49423433 | Common:1; Rare:53 | ||||
| chr15:49620769-49621099 | Common:6; Rare:126 | ||||
| chr15:50354860-50354998 | Rare:20 | ||||
| chr15:50355099-50355472 | Common:3; Rare:136 | ||||
| chr15:50424345-50424477 | Common:1; Rare:61 | ||||
| chr15:50908597-50908751 | Common:1; Rare:60; Clinvar (benign):2 |