| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49828391-49828634 | Common:1; Rare:82 | ||||
| chr12:50085287-50085355 | Rare:16 | ||||
| chr12:50283481-50283664 | Common:2; Rare:57 | ||||
| chr12:50400749-50400968 | Rare:67 | ||||
| chr12:50763914-50764120 | Common:1; Rare:61 | ||||
| chr12:51048142-51048351 | Common:1; Rare:73 | ||||
| chr12:51270278-51270354 | Common:2; Rare:21 | ||||
| chr12:51270358-51270482 | Common:1; Rare:33 | ||||
| chr12:52051104-52051449 | Common:1; Rare:118 | ||||
| chr12:52949793-52950019 | Rare:52 | ||||
| chr12:53079365-53079663 | Common:2; Rare:90 | ||||
| chr12:53295400-53295578 | Common:2; Rare:60 | ||||
| chr12:53321254-53321434 | Common:1; Rare:71; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:53441497-53441785 | Common:1; Rare:79 | ||||
| chr12:53625986-53626178 | Common:1; Rare:46 |