| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:89243670-89244215 | Common:2; Rare:148; Clinvar:3 | ||||
| chr15:89244441-89244483 | Rare:7 | ||||
| chr15:89244649-89244690 | Common:1; Rare:6 | ||||
| chr15:89334489-89334613 | Rare:47 | ||||
| chr15:89334760-89335098 | Common:3; Rare:142 | ||||
| chr15:89575092-89575573 | Common:5; Rare:142 | ||||
| chr15:89654892-89655053 | Common:1; Rare:31 | ||||
| chr15:89655356-89655552 | Common:1; Rare:63; Clinvar (benign):2 | ||||
| chr15:89690642-89690871 | Common:4; Rare:61 | ||||
| chr15:89750764-89751011 | Common:3; Rare:116 | ||||
| chr15:89776532-89776693 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:89893694-89893788 | Rare:18 | ||||
| chr15:89893900-89894353 | Common:4; Rare:135 | ||||
| chr15:89912779-89913125 | Common:2; Rare:104 | ||||
| chr15:90001326-90001546 | Rare:61 |