| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:63779749-63779921 | Common:2; Rare:61; Clinvar (benign):1 | ||||
| chr12:63780093-63780169 | Rare:35; Clinvar (pathogenic):1 | ||||
| chr12:64222242-64222369 | Rare:41 | ||||
| chr12:64404151-64404564 | Common:3; Rare:153 | ||||
| chr12:64452041-64452174 | Common:1; Rare:48 | ||||
| chr12:64759194-64759500 | Common:1; Rare:94; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:65278621-65278938 | Common:1; Rare:111; Clinvar (benign):4 | ||||
| chr12:66130715-66130807 | Rare:33 | ||||
| chr12:66189005-66189342 | Rare:89; Clinvar:1 | ||||
| chr12:66302278-66302604 | Common:1; Rare:78 | ||||
| chr12:67269149-67269434 | Common:2; Rare:84 | ||||
| chr12:67269546-67269700 | Common:1; Rare:62 | ||||
| chr12:68332243-68332598 | Common:1; Rare:117 | ||||
| chr12:68610724-68611041 | Common:1; Rare:130 | ||||
| chr12:68686843-68687062 | Common:3; Rare:66 |