| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:95327259-95327341 | Rare:17 | ||||
| chr15:95327713-95327843 | Common:1; Rare:31 | ||||
| chr15:95329447-95329629 | Rare:31 | ||||
| chr15:95477694-95477940 | Common:1; Rare:44 | ||||
| chr15:96327297-96327426 | Common:3; Rare:20 | ||||
| chr15:96354041-96354376 | Common:4; Rare:71 | ||||
| chr15:98650776-98650841 | Rare:21 | ||||
| chr15:99806875-99807002 | Common:2; Rare:17 | ||||
| chr15:101961503-101961633 | Rare:3 | ||||
| chr16:707186-707308 | Rare:18 | ||||
| chr16:1073599-1073817 | Common:3; Rare:43 | ||||
| chr16:1200432-1200760 | Common:5; Rare:171; Clinvar:2; Clinvar (benign):12 | ||||
| chr16:1361735-1362269 | Common:4; Rare:260; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):9 | ||||
| chr16:2123506-2123650 | Rare:49 | ||||
| chr16:2171335-2171593 | Common:1; Rare:90 |