| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:88142032-88142390 | Rare:98; Clinvar:3 | ||||
| chr12:88580440-88580586 | Common:1; Rare:50 | ||||
| chr12:89352368-89352703 | Rare:90 | ||||
| chr12:89524708-89524869 | Common:1; Rare:30 | ||||
| chr12:89525885-89525951 | Common:1; Rare:21 | ||||
| chr12:89525977-89526020 | Rare:18 | ||||
| chr12:92929102-92929196 | Common:1; Rare:24 | ||||
| chr12:93377728-93377929 | Rare:54 | ||||
| chr12:93441876-93442141 | Common:2; Rare:86 | ||||
| chr12:93570827-93571075 | Rare:64 | ||||
| chr12:93571726-93571912 | Common:7; Rare:71 | ||||
| chr12:93677262-93677409 | Rare:32 | ||||
| chr12:94459814-94460043 | Common:3; Rare:64 | ||||
| chr12:95003593-95003820 | Common:3; Rare:94; Clinvar (benign):6 | ||||
| chr12:95217377-95217769 | Common:4; Rare:106 |