| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:65278603-65278787 | Common:1; Rare:58; Clinvar (benign):1 | ||||
| chr12:65824672-65824855 | Common:6; Rare:73 | ||||
| chr12:65824901-65825129 | Common:1; Rare:55 | ||||
| chr12:69470300-69470439 | Common:2; Rare:49 | ||||
| chr12:70243657-70243756 | Common:1; Rare:31 | ||||
| chr12:71663795-71663983 | Common:1; Rare:61 | ||||
| chr12:72272275-72272374 | Common:2; Rare:26 | ||||
| chr12:76031584-76031813 | Common:1; Rare:82 | ||||
| chr12:77065532-77065680 | Rare:45 | ||||
| chr12:79935087-79935391 | Rare:112 | ||||
| chr12:80937673-80937812 | Common:1; Rare:42 | ||||
| chr12:82358366-82358566 | Rare:88 | ||||
| chr12:82358739-82358899 | Common:3; Rare:82 | ||||
| chr12:88142054-88142325 | Rare:67; Clinvar:3 | ||||
| chr12:88580440-88580559 | Common:1; Rare:40 |