| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44536855-44537401 | Common:3; Rare:200 | ||||
| chr15:44663522-44663715 | Rare:105; Clinvar:13; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr15:44711347-44711607 | Rare:78; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45023052-45023260 | Common:3; Rare:55 | ||||
| chr15:45378450-45378680 | Common:4; Rare:64; Clinvar:1; Clinvar (benign):8 | ||||
| chr15:45587099-45587274 | Rare:30 | ||||
| chr15:45587289-45587828 | Common:3; Rare:174; Clinvar:7; Clinvar (benign):3 | ||||
| chr15:47184181-47184378 | Common:1; Rare:64 | ||||
| chr15:48178111-48178448 | Common:1; Rare:103 | ||||
| chr15:48331367-48331440 | Rare:22 | ||||
| chr15:48332123-48332359 | Common:2; Rare:88; Clinvar:1 | ||||
| chr15:48811067-48811351 | Rare:71; Clinvar:2 | ||||
| chr15:48877995-48878394 | Rare:148 | ||||
| chr15:49046297-49046605 | Common:2; Rare:113 | ||||
| chr15:49155528-49155845 | Common:2; Rare:108 |