| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6606291-6606931 | Common:11; Rare:566 | ||||
| chr12:6607157-6608726 | Common:38; Rare:807 | ||||
| chr12:6635277-6635774 | Common:6; Rare:176 | ||||
| chr12:6635860-6636160 | Common:15; Rare:347 | ||||
| chr12:6638547-6638949 | Common:4; Rare:155 | ||||
| chr12:6639108-6639490 | Common:15; Rare:371 | ||||
| chr12:6662828-6662954 | Common:1; Rare:31 | ||||
| chr12:6663071-6663495 | Common:10; Rare:504 | ||||
| chr12:6688720-6689263 | Rare:640 | ||||
| chr12:6689250-6689882 | Common:12; Rare:721 | ||||
| chr12:6723256-6723430 | Rare:20 | ||||
| chr12:6723410-6723810 | Common:2; Rare:119 | ||||
| chr12:6723740-6724434 | Common:13; Rare:730 | ||||
| chr12:6724586-6724716 | Rare:35 | ||||
| chr12:6749880-6750180 | Common:4; Rare:89 |