| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89708770-89709097 | Common:1; Rare:125 | ||||
| chr12:89709296-89709442 | Common:2; Rare:72 | ||||
| chr12:92929102-92929160 | Common:1; Rare:14 | ||||
| chr12:92929181-92929512 | Common:1; Rare:105 | ||||
| chr12:93377728-93377972 | Rare:80 | ||||
| chr12:93441876-93442112 | Common:2; Rare:80 | ||||
| chr12:93569683-93569985 | Common:2; Rare:57 | ||||
| chr12:93570260-93570421 | Common:1; Rare:30 | ||||
| chr12:93570827-93571096 | Rare:69 | ||||
| chr12:93571738-93571912 | Common:7; Rare:67 | ||||
| chr12:94459771-94460047 | Common:3; Rare:76 | ||||
| chr12:95003593-95003831 | Common:3; Rare:99; Clinvar (benign):6 | ||||
| chr12:95073403-95073653 | Common:2; Rare:85 | ||||
| chr12:95217357-95217840 | Common:6; Rare:131 | ||||
| chr12:95218164-95218267 | Common:2; Rare:25 |