| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:68820733-68821045 | Rare:93 | ||||
| chr15:68930365-68930540 | Common:2; Rare:59 | ||||
| chr15:69160336-69160662 | Common:4; Rare:101 | ||||
| chr15:69414184-69414356 | Rare:45 | ||||
| chr15:69452688-69453020 | Common:5; Rare:139 | ||||
| chr15:70097856-70098092 | Common:1; Rare:54 | ||||
| chr15:70892403-70892880 | Common:1; Rare:116 | ||||
| chr15:72117827-72117958 | Rare:46 | ||||
| chr15:72118015-72118443 | Common:3; Rare:148 | ||||
| chr15:72231114-72231412 | Common:2; Rare:93 | ||||
| chr15:72272638-72272855 | Common:2; Rare:62 | ||||
| chr15:72375958-72376124 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72686135-72686220 | Common:2; Rare:31; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73633166-73633545 | Common:1; Rare:147 | ||||
| chr15:73684123-73684414 | Rare:79 |