| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:63844654-63844759 | Rare:24 | ||||
| chr12:64222242-64222337 | Rare:32 | ||||
| chr12:64452036-64452175 | Common:1; Rare:52 | ||||
| chr12:64759170-64759667 | Common:3; Rare:149; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:65169437-65169593 | Common:1; Rare:50; Clinvar:1 | ||||
| chr12:66130718-66130861 | Rare:48 | ||||
| chr12:66189135-66189344 | Rare:65; Clinvar:1 | ||||
| chr12:67269149-67269386 | Common:1; Rare:69 | ||||
| chr12:67648618-67648776 | Common:1; Rare:45 | ||||
| chr12:68332276-68332631 | Common:1; Rare:113 | ||||
| chr12:68610724-68611041 | Common:1; Rare:130 | ||||
| chr12:68808070-68808241 | Common:1; Rare:56 | ||||
| chr12:68808834-68809027 | Rare:35 | ||||
| chr12:68933151-68933337 | Rare:60 | ||||
| chr12:69470305-69470464 | Common:3; Rare:58 |