| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:94459798-94460064 | Common:3; Rare:76 | ||||
| chr12:94615991-94616234 | Common:1; Rare:47 | ||||
| chr12:95003593-95003832 | Common:3; Rare:100; Clinvar (benign):6 | ||||
| chr12:95073407-95073653 | Common:2; Rare:84 | ||||
| chr12:95217370-95217835 | Common:5; Rare:126 | ||||
| chr12:95218165-95218276 | Common:2; Rare:26 | ||||
| chr12:95474006-95474330 | Common:2; Rare:137 | ||||
| chr12:95548796-95548924 | Common:3; Rare:46 | ||||
| chr12:95858822-95859033 | Common:2; Rare:57 | ||||
| chr12:96194266-96194556 | Common:4; Rare:100 | ||||
| chr12:96399371-96399480 | Common:1; Rare:33 | ||||
| chr12:96400047-96400088 | Rare:15 | ||||
| chr12:96400436-96400682 | Common:1; Rare:109 | ||||
| chr12:96907195-96907293 | Rare:38 | ||||
| chr12:98515475-98515716 | Rare:73; Clinvar:1 |