| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:66386703-66386950 | Common:2; Rare:97; Clinvar:3; Clinvar (benign):4 | ||||
| chr15:66504786-66505154 | Common:1; Rare:140 | ||||
| chr15:67254623-67254828 | Rare:74 | ||||
| chr15:68817615-68817663 | Rare:13 | ||||
| chr15:69160342-69160605 | Common:3; Rare:72 | ||||
| chr15:69298802-69298967 | Common:3; Rare:40 | ||||
| chr15:69414209-69414448 | Rare:81 | ||||
| chr15:70892381-70892655 | Common:1; Rare:64 | ||||
| chr15:72118167-72118420 | Common:2; Rare:78 | ||||
| chr15:72231107-72231516 | Common:3; Rare:129 | ||||
| chr15:72375964-72376122 | Common:1; Rare:67; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr15:72686116-72686220 | Common:2; Rare:39; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73926322-73926466 | Rare:40 | ||||
| chr15:73994587-73994767 | Rare:36 | ||||
| chr15:74461107-74461298 | Rare:61 |