| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57227598-57227922 | Common:4; Rare:108 | ||||
| chr3:57555987-57556356 | Rare:105 | ||||
| chr3:57597286-57597832 | Common:7; Rare:165 | ||||
| chr3:57889885-57890099 | Rare:48; Clinvar (benign):2 | ||||
| chr3:58008323-58008439 | Common:1; Rare:45; Clinvar:1 | ||||
| chr3:58008553-58008736 | Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:58306472-58306574 | Common:3; Rare:41 | ||||
| chr3:58332768-58332973 | Common:6; Rare:57 | ||||
| chr3:58433794-58434126 | Common:2; Rare:106; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:61251383-61251594 | Common:4; Rare:53 | ||||
| chr3:61561412-61561649 | Common:2; Rare:83 | ||||
| chr3:62318941-62319049 | Rare:41 | ||||
| chr3:63863777-63864175 | Common:8; Rare:130 | ||||
| chr3:63911984-63912116 | Rare:41 | ||||
| chr3:64268108-64268333 | Rare:54 |