| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46372674-46372966 | Rare:123 | ||||
| chr12:47079511-47079804 | Common:1; Rare:71 | ||||
| chr12:47705962-47706088 | Rare:57 | ||||
| chr12:47758721-47759011 | Common:1; Rare:54 | ||||
| chr12:47904992-47905119 | Common:1; Rare:35; Clinvar:1 | ||||
| chr12:48105997-48106104 | Rare:29 | ||||
| chr12:48350790-48350963 | Rare:63 | ||||
| chr12:48351248-48351479 | Common:2; Rare:45 | ||||
| chr12:48716679-48717008 | Common:4; Rare:98 | ||||
| chr12:49018736-49018888 | Rare:64 | ||||
| chr12:49110646-49110821 | Rare:38 | ||||
| chr12:49131301-49131609 | Common:2; Rare:124 | ||||
| chr12:49188986-49189153 | Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264781-49265096 | Common:4; Rare:114 | ||||
| chr12:49367202-49367530 | Common:1; Rare:90 |