| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55973593-55973799 | Common:1; Rare:51 | ||||
| chr12:55997127-55997333 | Common:1; Rare:62; Clinvar:2 | ||||
| chr12:56007616-56007881 | Common:2; Rare:65 | ||||
| chr12:56020825-56021161 | Rare:61 | ||||
| chr12:56021170-56021599 | Common:10; Rare:104 | ||||
| chr12:56021601-56021908 | Common:2; Rare:51 | ||||
| chr12:56041608-56041968 | Common:4; Rare:84; Clinvar (benign):1 | ||||
| chr12:56042069-56042423 | Common:3; Rare:139; Clinvar:1; Clinvar (benign):5 | ||||
| chr12:56104401-56104674 | Common:4; Rare:102 | ||||
| chr12:56116272-56116714 | Common:3; Rare:158 | ||||
| chr12:56116906-56117206 | Common:4; Rare:78 | ||||
| chr12:56118076-56118318 | Common:1; Rare:79 | ||||
| chr12:56152455-56152669 | Rare:63 | ||||
| chr12:56157141-56157509 | Rare:86 | ||||
| chr12:56158084-56158438 | Common:1; Rare:109 |