| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:66356645-66356798 | Rare:48 | ||||
| chr15:66386676-66386961 | Common:2; Rare:112; Clinvar:3; Clinvar (benign):4 | ||||
| chr15:66499919-66500198 | Common:1; Rare:81 | ||||
| chr15:66504603-66505368 | Common:5; Rare:293 | ||||
| chr15:66702069-66702528 | Common:3; Rare:150 | ||||
| chr15:67065404-67065849 | Common:1; Rare:153 | ||||
| chr15:67137889-67138027 | Common:1; Rare:22; Clinvar:1 | ||||
| chr15:67254546-67254902 | Common:1; Rare:142 | ||||
| chr15:67520923-67521239 | Common:5; Rare:110 | ||||
| chr15:67521524-67521684 | Common:1; Rare:42 | ||||
| chr15:67542600-67542715 | Rare:35 | ||||
| chr15:68277645-68277879 | Common:6; Rare:66 | ||||
| chr15:68278013-68278133 | Rare:39 | ||||
| chr15:68817521-68817887 | Common:3; Rare:114 | ||||
| chr15:68820747-68820936 | Rare:67 |