| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120086986-120087325 | Common:1; Rare:73 | ||||
| chr12:120291893-120292219 | Common:9; Rare:130 | ||||
| chr12:120293234-120293488 | Common:2; Rare:105 | ||||
| chr12:120317453-120317880 | Common:4; Rare:103 | ||||
| chr12:120498436-120498736 | Rare:45 | ||||
| chr12:121663892-121664135 | Common:1; Rare:55 | ||||
| chr12:122063228-122063440 | Rare:31 | ||||
| chr12:122064105-122064426 | Common:2; Rare:51 | ||||
| chr12:122423665-122423935 | Common:1; Rare:39 | ||||
| chr12:123261755-123261879 | Common:2; Rare:25 | ||||
| chr12:123618517-123618836 | Rare:95 | ||||
| chr12:123900887-123901008 | Common:2; Rare:16 | ||||
| chr12:123908818-123909159 | Common:6; Rare:70 | ||||
| chr12:123909173-123909307 | Common:2; Rare:36; Clinvar (benign):1 | ||||
| chr12:123909511-123909628 | Rare:29 |