| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:60397886-60398271 | Common:7; Rare:190 | ||||
| chr15:60398566-60399533 | Common:38; Rare:303 | ||||
| chr15:60478878-60479347 | Common:12; Rare:431 | ||||
| chr15:60592410-60592980 | Common:12; Rare:330 | ||||
| chr15:61229196-61229506 | Common:1; Rare:74 | ||||
| chr15:62059358-62060167 | Common:9; Rare:336 | ||||
| chr15:62060262-62060711 | Common:1; Rare:298 | ||||
| chr15:62066784-62067034 | Common:2; Rare:81 | ||||
| chr15:62390375-62390676 | Common:2; Rare:340 | ||||
| chr15:63042351-63043160 | Common:21; Rare:461; Clinvar:23; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr15:63043132-63043467 | Rare:124 | ||||
| chr15:63048150-63048690 | Common:14; Rare:459; Clinvar:10; Clinvar (benign):9 | ||||
| chr15:63049060-63049570 | Common:5; Rare:116 | ||||
| chr15:63121648-63121951 | Common:7; Rare:218; Clinvar (benign):2 | ||||
| chr15:63122120-63122700 | Common:8; Rare:274 |