| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:88467226-88467801 | Common:15; Rare:518 | ||||
| chr15:88546240-88546464 | Common:6; Rare:146 | ||||
| chr15:88546480-88546900 | Rare:350 | ||||
| chr15:88621074-88621459 | Common:9; Rare:336 | ||||
| chr15:88621457-88621857 | Common:5; Rare:101 | ||||
| chr15:88636102-88636329 | Common:4; Rare:60 | ||||
| chr15:88638629-88639288 | Common:4; Rare:385 | ||||
| chr15:88913000-88913280 | Common:8; Rare:112 | ||||
| chr15:88913322-88913583 | Common:5; Rare:152 | ||||
| chr15:88913563-88914056 | Common:6; Rare:155 | ||||
| chr15:89088032-89088613 | Common:15; Rare:341 | ||||
| chr15:89115834-89116187 | Rare:67 | ||||
| chr15:89243758-89244117 | Common:4; Rare:249; Clinvar:9 | ||||
| chr15:89244266-89244960 | Common:14; Rare:260 | ||||
| chr15:89334690-89335129 | Common:8; Rare:402; Clinvar:2; Clinvar (benign):1 |