| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48925330-48925681 | Common:1; Rare:107 | ||||
| chr12:48926000-48926064 | Rare:4 | ||||
| chr12:48956438-48956746 | Common:3; Rare:53 | ||||
| chr12:48957358-48957682 | Common:4; Rare:89 | ||||
| chr12:48999439-48999483 | Rare:6 | ||||
| chr12:49018000-49018304 | Rare:50 | ||||
| chr12:49018371-49018696 | Common:3; Rare:71 | ||||
| chr12:49018700-49018960 | Common:1; Rare:109 | ||||
| chr12:49059142-49059449 | Rare:56 | ||||
| chr12:49060230-49060337 | Rare:32 | ||||
| chr12:49069591-49069700 | Common:1; Rare:24 | ||||
| chr12:49069858-49070217 | Common:2; Rare:85 | ||||
| chr12:49110032-49110292 | Common:2; Rare:60 | ||||
| chr12:49110540-49110693 | Rare:40 | ||||
| chr12:49110766-49111083 | Rare:77 |