| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:66293484-66293854 | Common:4; Rare:115 | ||||
| chr15:66386667-66386958 | Common:2; Rare:113; Clinvar:3; Clinvar (benign):4 | ||||
| chr15:66500054-66500379 | Common:1; Rare:102 | ||||
| chr15:66504786-66505188 | Common:2; Rare:151 | ||||
| chr15:67065815-67066235 | Common:3; Rare:115; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr15:67254358-67254425 | Rare:13 | ||||
| chr15:67254559-67254888 | Common:1; Rare:129 | ||||
| chr15:67521020-67521457 | Common:6; Rare:182 | ||||
| chr15:67521567-67521865 | Rare:81 | ||||
| chr15:67542597-67542774 | Common:2; Rare:62 | ||||
| chr15:67543243-67543347 | Rare:33 | ||||
| chr15:68197517-68197757 | Rare:77 | ||||
| chr15:68205260-68205344 | Rare:31 | ||||
| chr15:68277645-68277823 | Common:4; Rare:51 | ||||
| chr15:68817455-68817709 | Common:1; Rare:82 |