| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:65959439-65959678 | Common:2; Rare:34 | ||||
| chr12:66128553-66128834 | Common:3; Rare:36 | ||||
| chr12:66141894-66141939 | Rare:5 | ||||
| chr12:66153355-66153653 | Common:4; Rare:68 | ||||
| chr12:66167476-66167677 | Common:1; Rare:28 | ||||
| chr12:67297538-67297779 | Rare:56 | ||||
| chr12:67657019-67657190 | Rare:57 | ||||
| chr12:68615658-68615885 | Common:1; Rare:48 | ||||
| chr12:68831221-68831487 | Common:1; Rare:65 | ||||
| chr12:69588556-69588639 | Rare:17 | ||||
| chr12:69597634-69598067 | Common:5; Rare:98; Clinvar:2 | ||||
| chr12:69601275-69601300 | Rare:10 | ||||
| chr12:70353373-70353485 | Common:2; Rare:18 | ||||
| chr12:72255401-72255565 | Common:2; Rare:35 | ||||
| chr12:72262343-72262496 | Rare:28 |