| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41660550-41660990 | Common:2; Rare:351 | ||||
| chr15:41773870-41774220 | Common:3; Rare:90 | ||||
| chr15:41774289-41774700 | Common:4; Rare:309 | ||||
| chr15:41827818-41828218 | Common:15; Rare:403 | ||||
| chr15:41828220-41828420 | Common:2; Rare:74 | ||||
| chr15:41972421-41973001 | Common:18; Rare:950 | ||||
| chr15:42207863-42208549 | Common:1; Rare:338 | ||||
| chr15:42272960-42273300 | Common:7; Rare:578 | ||||
| chr15:42273320-42273730 | Common:3; Rare:619 | ||||
| chr15:42273826-42273965 | Common:1; Rare:23 | ||||
| chr15:42274224-42274624 | Rare:133 | ||||
| chr15:42274627-42275027 | Common:2; Rare:87 | ||||
| chr15:42275060-42275837 | Common:11; Rare:195 | ||||
| chr15:42401521-42402646 | Common:10; Rare:442; Clinvar:31; Clinvar (benign):5; Clinvar (pathogenic):29 | ||||
| chr15:42404228-42404877 | Common:1; Rare:157 |