| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109154544-109154748 | Common:1; Rare:54 | ||||
| chr12:109477260-109477735 | Common:4; Rare:126 | ||||
| chr12:109573099-109573312 | Common:2; Rare:47 | ||||
| chr12:109573421-109573847 | Common:5; Rare:143; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr12:109880327-109880758 | Common:2; Rare:124 | ||||
| chr12:109900102-109900679 | Rare:143 | ||||
| chr12:109900889-109901171 | Common:1; Rare:59 | ||||
| chr12:109996175-109996472 | Common:2; Rare:86 | ||||
| chr12:109998874-109999523 | Rare:137 | ||||
| chr12:110048389-110048800 | Common:2; Rare:99 | ||||
| chr12:110049149-110049297 | Common:1; Rare:31 | ||||
| chr12:110124116-110124515 | Common:2; Rare:118 | ||||
| chr12:110280495-110280672 | Rare:46 | ||||
| chr12:110280954-110281375 | Common:1; Rare:160; Clinvar (benign):1 | ||||
| chr12:110281926-110282000 | Rare:23 |