| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:92145396-92145656 | Common:2; Rare:109 | ||||
| chr12:92145822-92146224 | Common:2; Rare:131 | ||||
| chr12:92929119-92929476 | Common:2; Rare:105 | ||||
| chr12:93377549-93377943 | Rare:127 | ||||
| chr12:93378117-93378419 | Common:1; Rare:72 | ||||
| chr12:93441863-93442136 | Common:2; Rare:87 | ||||
| chr12:93467440-93467554 | Common:1; Rare:35 | ||||
| chr12:93570827-93571078 | Rare:65 | ||||
| chr12:93571713-93571912 | Common:7; Rare:77 | ||||
| chr12:93677315-93677399 | Rare:18 | ||||
| chr12:94459765-94460064 | Common:3; Rare:84 | ||||
| chr12:95003593-95003813 | Common:3; Rare:93; Clinvar (benign):6 | ||||
| chr12:95217299-95217886 | Common:6; Rare:156 | ||||
| chr12:95218164-95218306 | Common:2; Rare:37 | ||||
| chr12:95473970-95474330 | Common:2; Rare:147 |