| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:59104927-59105178 | Common:1; Rare:89 | ||||
| chr15:59372506-59373045 | Common:4; Rare:177 | ||||
| chr15:59689219-59689606 | Common:10; Rare:186 | ||||
| chr15:60351134-60351295 | Rare:50 | ||||
| chr15:60351715-60351910 | Common:2; Rare:57 | ||||
| chr15:60397098-60397389 | Rare:67 | ||||
| chr15:60397829-60398097 | Common:3; Rare:73 | ||||
| chr15:60398547-60398770 | Common:2; Rare:51 | ||||
| chr15:60479085-60479220 | Common:2; Rare:53 | ||||
| chr15:60592552-60592771 | Common:1; Rare:61 | ||||
| chr15:61229220-61229294 | Rare:12 | ||||
| chr15:62060349-62060533 | Rare:73 | ||||
| chr15:62758328-62758618 | Common:3; Rare:46 | ||||
| chr15:63042345-63042487 | Common:2; Rare:41 | ||||
| chr15:63042502-63043313 | Common:5; Rare:217; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):1 |