| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:66293475-66293631 | Common:4; Rare:51 | ||||
| chr15:66356641-66356840 | Rare:63 | ||||
| chr15:66386676-66386950 | Common:2; Rare:104; Clinvar:3; Clinvar (benign):4 | ||||
| chr15:66500058-66500393 | Common:1; Rare:106 | ||||
| chr15:66504788-66505158 | Common:2; Rare:140 | ||||
| chr15:67063949-67064132 | Common:2; Rare:33 | ||||
| chr15:67065381-67065671 | Common:1; Rare:102 | ||||
| chr15:67065874-67066207 | Common:3; Rare:89; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr15:67254559-67254850 | Common:1; Rare:108 | ||||
| chr15:67521037-67521251 | Common:4; Rare:94 | ||||
| chr15:67542604-67542764 | Common:2; Rare:56 | ||||
| chr15:67543202-67543328 | Rare:38 | ||||
| chr15:68197450-68197851 | Common:1; Rare:121 | ||||
| chr15:68205256-68205365 | Common:1; Rare:41 | ||||
| chr15:68277491-68277795 | Common:5; Rare:104 |