| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:75368579-75368923 | Rare:94 | ||||
| chr15:75455801-75455967 | Rare:52 | ||||
| chr15:75578736-75578895 | Rare:54 | ||||
| chr15:75625612-75625887 | Common:2; Rare:63 | ||||
| chr15:75640115-75640386 | Common:1; Rare:94 | ||||
| chr15:75647820-75647968 | Common:1; Rare:30 | ||||
| chr15:75723903-75724051 | Common:1; Rare:29 | ||||
| chr15:75843268-75843675 | Common:1; Rare:153 | ||||
| chr15:75903812-75903961 | Rare:61 | ||||
| chr15:76286403-76286691 | Common:2; Rare:65; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:76311352-76311630 | Common:1; Rare:94; Clinvar:6; Clinvar (benign):8 | ||||
| chr15:77070923-77071377 | Common:2; Rare:152 | ||||
| chr15:77420046-77420486 | Common:2; Rare:130 | ||||
| chr15:77420874-77420962 | Rare:27 | ||||
| chr15:77421123-77421360 | Common:1; Rare:57 |