| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:82358736-82358875 | Common:3; Rare:74 | ||||
| chr12:88035435-88035615 | Common:1; Rare:60 | ||||
| chr12:88142060-88142368 | Rare:84; Clinvar:3 | ||||
| chr12:89524756-89524883 | Common:1; Rare:23 | ||||
| chr12:89525986-89526088 | Rare:36 | ||||
| chr12:89708813-89709106 | Common:1; Rare:114 | ||||
| chr12:89709290-89709391 | Common:2; Rare:51 | ||||
| chr12:92145841-92146211 | Common:2; Rare:111 | ||||
| chr12:93441864-93442186 | Common:2; Rare:100 | ||||
| chr12:93467739-93467765 | Common:1; Rare:5 | ||||
| chr12:93677312-93677398 | Rare:18 | ||||
| chr12:94459833-94460064 | Common:2; Rare:69 | ||||
| chr12:95003680-95003746 | Common:2; Rare:29; Clinvar (benign):3 | ||||
| chr12:95217427-95217769 | Common:3; Rare:92 | ||||
| chr12:95473933-95473957 | Rare:7 |