| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:85794849-85795155 | Common:1; Rare:101 | ||||
| chr15:88467228-88467785 | Common:10; Rare:388 | ||||
| chr15:88621172-88621430 | Common:6; Rare:181 | ||||
| chr15:88638668-88639117 | Common:2; Rare:210 | ||||
| chr15:89088120-89088546 | Common:10; Rare:190 | ||||
| chr15:89243878-89244473 | Common:6; Rare:207; Clinvar:6 | ||||
| chr15:89244550-89244860 | Common:3; Rare:112 | ||||
| chr15:89334320-89334670 | Common:5; Rare:152; Clinvar:1 | ||||
| chr15:89334735-89335069 | Common:4; Rare:228; Clinvar:1 | ||||
| chr15:89575120-89575570 | Common:8; Rare:261 | ||||
| chr15:89690681-89690829 | Common:5; Rare:80 | ||||
| chr15:89750797-89750996 | Common:4; Rare:189 | ||||
| chr15:89776410-89776950 | Common:16; Rare:333; Clinvar:10; Clinvar (benign):15; Clinvar (pathogenic):13 | ||||
| chr15:89893922-89894136 | Common:4; Rare:117 | ||||
| chr15:89912809-89912990 | Common:4; Rare:117 |