| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:78979520-78979629 | Rare:15 | ||||
| chr15:79310766-79311328 | Common:6; Rare:164 | ||||
| chr15:79896667-79897238 | Common:12; Rare:216; Clinvar (pathogenic):1 | ||||
| chr15:79923036-79923403 | Common:4; Rare:150 | ||||
| chr15:79923594-79924110 | Common:9; Rare:189 | ||||
| chr15:79970716-79970907 | Common:2; Rare:44 | ||||
| chr15:79971046-79971387 | Common:2; Rare:61 | ||||
| chr15:80059383-80060053 | Common:2; Rare:236 | ||||
| chr15:80152894-80153064 | Common:2; Rare:39; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:80694957-80695347 | Common:3; Rare:122 | ||||
| chr15:80695713-80695729 | Rare:4 | ||||
| chr15:80989559-80989629 | Rare:20 | ||||
| chr15:80989738-80990093 | Common:5; Rare:151 | ||||
| chr15:81000555-81000574 | Rare:1 | ||||
| chr15:81000702-81001227 | Common:1; Rare:165 |