| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:62874072-62874293 | Common:1; Rare:52 | ||||
| chr3:66386375-66386619 | Common:3; Rare:63 | ||||
| chr3:66394141-66394343 | Common:2; Rare:47; Clinvar (benign):1 | ||||
| chr3:67000090-67000165 | Rare:14 | ||||
| chr3:67016925-67017219 | Common:3; Rare:64 | ||||
| chr3:67018417-67018654 | Rare:38 | ||||
| chr3:67030796-67030991 | Rare:38 | ||||
| chr3:67653674-67653769 | Common:1; Rare:30 | ||||
| chr3:67655333-67655908 | Common:1; Rare:203 | ||||
| chr3:67685679-67685746 | Rare:11 | ||||
| chr3:69079306-69079482 | Rare:25 | ||||
| chr3:69081700-69081825 | Rare:20 | ||||
| chr3:69082917-69083151 | Rare:30 | ||||
| chr3:69086176-69086364 | Rare:23 | ||||
| chr3:69088126-69088273 | Rare:31 |