| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:94459798-94460047 | Common:3; Rare:70 | ||||
| chr12:95003605-95003819 | Common:3; Rare:89; Clinvar (benign):6 | ||||
| chr12:95073416-95073654 | Common:2; Rare:82 | ||||
| chr12:95217299-95217849 | Common:6; Rare:148 | ||||
| chr12:95218160-95218313 | Common:2; Rare:38 | ||||
| chr12:95473992-95474330 | Common:2; Rare:140 | ||||
| chr12:95548796-95548924 | Common:3; Rare:46 | ||||
| chr12:95790761-95791135 | Common:2; Rare:88 | ||||
| chr12:95943217-95943500 | Common:3; Rare:64 | ||||
| chr12:96013748-96013994 | Common:1; Rare:57 | ||||
| chr12:96035363-96035759 | Common:3; Rare:99 | ||||
| chr12:96400541-96400756 | Rare:87 | ||||
| chr12:96907164-96907450 | Common:2; Rare:95 | ||||
| chr12:98515471-98515697 | Rare:71; Clinvar:1 | ||||
| chr12:98515793-98515870 | Rare:38; Clinvar:3; Clinvar (benign):1 |