| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40930516-40930916 | Rare:136 | ||||
| chr15:40952895-40953004 | Rare:31 | ||||
| chr15:40953111-40953594 | Common:12; Rare:616 | ||||
| chr15:41115502-41116810 | Common:18; Rare:1593 | ||||
| chr15:41116733-41117341 | Rare:134 | ||||
| chr15:41230588-41230994 | Common:1; Rare:360 | ||||
| chr15:41230904-41231657 | Common:3; Rare:684; Clinvar (pathogenic):3 | ||||
| chr15:41331756-41332373 | Common:9; Rare:401 | ||||
| chr15:41332452-41333045 | Common:8; Rare:744 | ||||
| chr15:41333205-41333689 | Common:3; Rare:179 | ||||
| chr15:41401995-41402395 | Common:3; Rare:159; Clinvar:8 | ||||
| chr15:41402371-41402675 | Common:18; Rare:347; Clinvar:2; Clinvar (benign):3 | ||||
| chr15:41402857-41403281 | Common:2; Rare:178 | ||||
| chr15:41416333-41416733 | Common:3; Rare:96 | ||||
| chr15:41416706-41416810 | Rare:21 |