| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:92145836-92146224 | Common:2; Rare:120 | ||||
| chr12:93377728-93377957 | Rare:75 | ||||
| chr12:93378190-93378381 | Common:1; Rare:45 | ||||
| chr12:93441880-93442136 | Common:2; Rare:83 | ||||
| chr12:93570245-93570429 | Common:1; Rare:38 | ||||
| chr12:93570826-93571075 | Rare:65 | ||||
| chr12:93571400-93571507 | Rare:21 | ||||
| chr12:93571709-93571912 | Common:7; Rare:79 | ||||
| chr12:93572513-93572526 | |||||
| chr12:94459833-94460047 | Common:2; Rare:63 | ||||
| chr12:95003629-95003833 | Common:3; Rare:81; Clinvar (benign):4 | ||||
| chr12:95217386-95217769 | Common:4; Rare:105 | ||||
| chr12:95474037-95474191 | Common:2; Rare:73 | ||||
| chr12:95548798-95548924 | Common:3; Rare:45 | ||||
| chr12:95858822-95859033 | Common:2; Rare:57 |