| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:23039534-23039695 | Common:1; Rare:66 | ||||
| chr15:23565481-23565723 | Common:2; Rare:73 | ||||
| chr15:23566200-23566473 | Common:1; Rare:123; Clinvar (pathogenic):1 | ||||
| chr15:23647847-23647931 | Rare:25 | ||||
| chr15:23687237-23687406 | Common:1; Rare:60 | ||||
| chr15:24823438-24823716 | Common:2; Rare:63; Clinvar:1 | ||||
| chr15:24856474-24856685 | Common:2; Rare:51 | ||||
| chr15:24954746-24955062 | Common:1; Rare:129 | ||||
| chr15:25438984-25439227 | Common:2; Rare:91 | ||||
| chr15:26773722-26773825 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr15:30903777-30903943 | Rare:43 | ||||
| chr15:31870561-31870913 | Rare:104 | ||||
| chr15:32030359-32030606 | Common:7; Rare:91 | ||||
| chr15:32615104-32615603 | Common:7; Rare:126 | ||||
| chr15:32641534-32641632 | Rare:24 |