| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:13000230-13000445 | Common:1; Rare:72 | ||||
| chr12:14803395-14803699 | Common:3; Rare:83 | ||||
| chr12:15882289-15882728 | Common:1; Rare:150 | ||||
| chr12:16606482-16606623 | Rare:38 | ||||
| chr12:21501540-21501915 | Common:4; Rare:104 | ||||
| chr12:26938327-26938516 | Common:1; Rare:71 | ||||
| chr12:27332705-27332945 | Common:2; Rare:73 | ||||
| chr12:27710702-27710886 | Common:2; Rare:76 | ||||
| chr12:31729019-31729265 | Rare:72 | ||||
| chr12:32896738-32896867 | Common:2; Rare:44; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:38905589-38905710 | Common:3; Rare:32 | ||||
| chr12:42326030-42326205 | Common:1; Rare:57 | ||||
| chr12:43758753-43759005 | Common:2; Rare:71; Clinvar:2 | ||||
| chr12:45215989-45216147 | Common:1; Rare:53 | ||||
| chr12:46268613-46268807 | Common:1; Rare:54 |