| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6752927-6753194 | Common:6; Rare:83 | ||||
| chr12:6765927-6766363 | Common:2; Rare:81 | ||||
| chr12:6766478-6766747 | Rare:73 | ||||
| chr12:6829644-6829952 | Common:2; Rare:80 | ||||
| chr12:6851217-6851497 | Rare:66 | ||||
| chr12:6851913-6852199 | Rare:75 | ||||
| chr12:6867460-6867671 | Common:2; Rare:108; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6870048-6870309 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6873230-6873772 | Common:5; Rare:147 | ||||
| chr12:6914207-6914589 | Rare:89 | ||||
| chr12:6927887-6928372 | Common:3; Rare:109 | ||||
| chr12:6943874-6944305 | Common:12; Rare:376; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:6946342-6946736 | Common:2; Rare:121 | ||||
| chr12:6967505-6967919 | Rare:133 | ||||
| chr12:6970200-6971090 | Common:10; Rare:292; Clinvar (benign):2 |