| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:96906759-96906987 | Common:5; Rare:40 | ||||
| chr12:96907102-96907359 | Common:3; Rare:95 | ||||
| chr12:96907372-96907492 | Rare:24 | ||||
| chr12:98515115-98515131 | Rare:2 | ||||
| chr12:98515136-98515359 | Common:3; Rare:58 | ||||
| chr12:98515363-98515785 | Common:1; Rare:143; Clinvar:2 | ||||
| chr12:98515967-98516144 | Common:2; Rare:76; Clinvar:4; Clinvar (benign):8 | ||||
| chr12:98516242-98516574 | Common:2; Rare:105 | ||||
| chr12:98593005-98593098 | Common:1; Rare:24 | ||||
| chr12:98593378-98593913 | Common:2; Rare:172; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644438-98644559 | Rare:40 | ||||
| chr12:98644695-98645397 | Common:8; Rare:210 | ||||
| chr12:98645789-98645977 | Rare:30 | ||||
| chr12:99984577-99984765 | Rare:68 | ||||
| chr12:99984767-99985093 | Common:3; Rare:84 |