| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:92145797-92146239 | Common:4; Rare:154 | ||||
| chr12:92929218-92929517 | Common:1; Rare:94 | ||||
| chr12:93377709-93377956 | Rare:83 | ||||
| chr12:93378190-93378419 | Common:1; Rare:54 | ||||
| chr12:93441859-93442141 | Common:2; Rare:90 | ||||
| chr12:93570826-93571085 | Rare:67 | ||||
| chr12:93571728-93571912 | Common:7; Rare:70 | ||||
| chr12:94459802-94460043 | Common:3; Rare:68 | ||||
| chr12:95003593-95003811 | Common:3; Rare:93; Clinvar (benign):6 | ||||
| chr12:95217377-95217849 | Common:4; Rare:128 | ||||
| chr12:95474005-95474203 | Common:2; Rare:93 | ||||
| chr12:95548796-95548928 | Common:3; Rare:47 | ||||
| chr12:95858822-95859033 | Common:2; Rare:57 | ||||
| chr12:98515355-98515653 | Common:1; Rare:104; Clinvar:1 | ||||
| chr12:98515836-98515882 | Rare:22; Clinvar (benign):1 |