| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:71686026-71686129 | Common:1; Rare:30 | ||||
| chr12:72272222-72272377 | Common:3; Rare:38 | ||||
| chr12:74537717-74537928 | Common:1; Rare:74 | ||||
| chr12:75390890-75391109 | Common:1; Rare:69 | ||||
| chr12:75480611-75480904 | Rare:62 | ||||
| chr12:76348354-76348480 | Common:1; Rare:47; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559715-76559893 | Rare:72 | ||||
| chr12:79690510-79690705 | Common:1; Rare:58 | ||||
| chr12:79934791-79935388 | Common:1; Rare:214 | ||||
| chr12:80937688-80937859 | Common:1; Rare:53 | ||||
| chr12:81077772-81078114 | Rare:71 | ||||
| chr12:82358338-82358556 | Rare:101 | ||||
| chr12:82358727-82358915 | Common:3; Rare:94 | ||||
| chr12:85036275-85036371 | Rare:25 | ||||
| chr12:88142027-88142373 | Rare:97; Clinvar:3 |