| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57772087-57772220 | Rare:51 | ||||
| chr12:57772520-57772670 | Common:3; Rare:22 | ||||
| chr12:58920137-58920340 | Common:2; Rare:63 | ||||
| chr12:58920491-58920657 | Common:2; Rare:58 | ||||
| chr12:62260165-62260420 | Common:1; Rare:91 | ||||
| chr12:62934041-62934324 | Common:1; Rare:58 | ||||
| chr12:63779760-63779921 | Common:2; Rare:56; Clinvar (benign):1 | ||||
| chr12:64222248-64222372 | Rare:38 | ||||
| chr12:64404246-64404639 | Common:5; Rare:142 | ||||
| chr12:64452034-64452171 | Common:1; Rare:50 | ||||
| chr12:64759160-64759496 | Common:1; Rare:108; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:65169433-65169602 | Common:1; Rare:52; Clinvar:1 | ||||
| chr12:66130686-66130861 | Rare:63 | ||||
| chr12:68332265-68332375 | Rare:49 | ||||
| chr12:68610695-68610979 | Common:1; Rare:127 |