| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95003616-95003835 | Common:3; Rare:91; Clinvar (benign):5 | ||||
| chr12:95025190-95025340 | Common:1; Rare:35 | ||||
| chr12:95217372-95217884 | Common:5; Rare:138 | ||||
| chr12:95218100-95218321 | Common:2; Rare:57 | ||||
| chr12:95474061-95474328 | Common:2; Rare:114 | ||||
| chr12:96035366-96035412 | Rare:11 | ||||
| chr12:96035487-96035751 | Common:2; Rare:64 | ||||
| chr12:96399369-96399503 | Common:1; Rare:42 | ||||
| chr12:98515431-98515675 | Rare:83; Clinvar:1 | ||||
| chr12:98515811-98516144 | Common:2; Rare:135; Clinvar:8; Clinvar (benign):10 | ||||
| chr12:98593585-98594131 | Common:1; Rare:189; Clinvar:7; Clinvar (benign):7 | ||||
| chr12:98644526-98644583 | Rare:24 | ||||
| chr12:98644712-98644843 | Common:3; Rare:44 | ||||
| chr12:100142835-100143013 | Common:2; Rare:66 | ||||
| chr12:100199888-100200066 | Common:1; Rare:37 |