| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:59689145-59689408 | Common:5; Rare:114 | ||||
| chr15:60397183-60397217 | Rare:6 | ||||
| chr15:60397887-60398134 | Common:3; Rare:61 | ||||
| chr15:60478917-60479247 | Common:4; Rare:142 | ||||
| chr15:61229205-61229449 | Common:1; Rare:55 | ||||
| chr15:62060273-62060539 | Rare:98 | ||||
| chr15:62066865-62067027 | Common:1; Rare:25 | ||||
| chr15:62165247-62165428 | Common:1; Rare:46 | ||||
| chr15:62390434-62390664 | Common:1; Rare:105 | ||||
| chr15:62561151-62561431 | Common:2; Rare:74 | ||||
| chr15:62835726-62836036 | Common:2; Rare:110 | ||||
| chr15:63042505-63042948 | Common:4; Rare:137; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:63043050-63043227 | Common:1; Rare:28 | ||||
| chr15:63048268-63048707 | Common:5; Rare:164; Clinvar:5; Clinvar (benign):4 | ||||
| chr15:63055084-63055526 | Common:3; Rare:90 |