| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53625962-53626137 | Common:1; Rare:40 | ||||
| chr12:53626333-53626520 | Common:3; Rare:49 | ||||
| chr12:53984996-53985267 | Common:2; Rare:71 | ||||
| chr12:53986019-53986298 | Common:1; Rare:76 | ||||
| chr12:54016594-54016909 | Rare:74 | ||||
| chr12:54259535-54259676 | Rare:27 | ||||
| chr12:54280044-54280222 | Rare:60 | ||||
| chr12:55716383-55716588 | Common:3; Rare:56 | ||||
| chr12:55728952-55729214 | Rare:55 | ||||
| chr12:55829523-55829793 | Rare:88 | ||||
| chr12:55966682-55966843 | Rare:43 | ||||
| chr12:56041608-56041978 | Common:4; Rare:84; Clinvar (benign):1 | ||||
| chr12:56152311-56152620 | Rare:85 | ||||
| chr12:56221855-56222026 | Common:1; Rare:43 | ||||
| chr12:56300013-56300133 | Common:1; Rare:49 |