| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:92929102-92929473 | Common:2; Rare:111 | ||||
| chr12:93377746-93377929 | Rare:45 | ||||
| chr12:93441888-93442173 | Common:2; Rare:91 | ||||
| chr12:93571761-93571902 | Common:6; Rare:57 | ||||
| chr12:94459833-94460041 | Common:2; Rare:61 | ||||
| chr12:95217376-95217866 | Common:4; Rare:132 | ||||
| chr12:95474006-95474191 | Common:2; Rare:87 | ||||
| chr12:95995894-95996098 | Common:2; Rare:37; Clinvar:2 | ||||
| chr12:95996260-95996497 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:96907162-96907290 | Common:1; Rare:45 | ||||
| chr12:98515353-98515716 | Common:1; Rare:121; Clinvar:1 | ||||
| chr12:98593477-98593791 | Common:2; Rare:102; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98645007-98645305 | Common:2; Rare:90 | ||||
| chr12:100200655-100200854 | Common:1; Rare:64 | ||||
| chr12:100267047-100267326 | Common:1; Rare:120 |