| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:64751604-64751820 | Rare:50 | ||||
| chr15:64774741-64774784 | Rare:14 | ||||
| chr15:68194048-68194238 | Rare:60 | ||||
| chr15:73927695-73927860 | Common:1; Rare:49 | ||||
| chr15:82372574-82372766 | Common:2; Rare:41 | ||||
| chr15:82372824-82372971 | Common:1; Rare:22 | ||||
| chr15:82750424-82750594 | Common:2; Rare:44 | ||||
| chr15:84570183-84570275 | Common:3; Rare:27 | ||||
| chr15:84631314-84631508 | Common:3; Rare:62 | ||||
| chr15:92882387-92882702 | Common:2; Rare:84 | ||||
| chr15:93000313-93000594 | Rare:65; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr15:93086326-93086616 | Common:1; Rare:65 | ||||
| chr15:95477715-95477883 | Common:1; Rare:27 | ||||
| chr15:96327324-96327566 | Common:3; Rare:35 | ||||
| chr15:97970948-97971179 | Common:3; Rare:61 |