| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:54429057-54429416 | Common:2; Rare:70 | ||||
| chr12:54432004-54432038 | Rare:2 | ||||
| chr12:54432104-54432410 | Common:2; Rare:55 | ||||
| chr12:55697215-55697477 | Common:2; Rare:70; Clinvar (benign):3 | ||||
| chr12:55709758-55709993 | Common:1; Rare:33 | ||||
| chr12:56132320-56132562 | Rare:72 | ||||
| chr12:56171278-56171640 | Common:2; Rare:82 | ||||
| chr12:56634993-56635117 | Rare:22 | ||||
| chr12:57177227-57177589 | Common:1; Rare:89 | ||||
| chr12:57195769-57196165 | Common:3; Rare:107 | ||||
| chr12:57204422-57204757 | Common:2; Rare:88 | ||||
| chr12:57211772-57212001 | Rare:54 | ||||
| chr12:57823601-57823914 | Rare:83 | ||||
| chr12:62603511-62603609 | Common:1; Rare:29 | ||||
| chr12:63821826-63821956 | Common:1; Rare:43 |