| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:66386695-66386940 | Common:2; Rare:96; Clinvar:2; Clinvar (benign):3 | ||||
| chr15:66504786-66505158 | Common:2; Rare:140 | ||||
| chr15:67254623-67254801 | Rare:67 | ||||
| chr15:67521585-67521664 | Rare:25 | ||||
| chr15:67542613-67542756 | Common:2; Rare:48 | ||||
| chr15:68205268-68205313 | Rare:15 | ||||
| chr15:69160335-69160670 | Common:4; Rare:101 | ||||
| chr15:69414209-69414366 | Rare:44 | ||||
| chr15:69452701-69453020 | Common:5; Rare:132 | ||||
| chr15:70892518-70892822 | Common:1; Rare:57 | ||||
| chr15:71547221-71547293 | Rare:14 | ||||
| chr15:72118167-72118435 | Common:2; Rare:88 | ||||
| chr15:72222541-72222670 | Rare:19 | ||||
| chr15:72231114-72231520 | Common:3; Rare:129 | ||||
| chr15:72375968-72376103 | Common:1; Rare:56; Clinvar:3; Clinvar (pathogenic):2 |