| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76084553-76085079 | Common:6; Rare:141 | ||||
| chr12:76348332-76348468 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559708-76559914 | Rare:80 | ||||
| chr12:76764040-76764281 | Common:2; Rare:101 | ||||
| chr12:76878948-76879127 | Rare:60 | ||||
| chr12:77065486-77065772 | Common:1; Rare:95 | ||||
| chr12:78864515-78864809 | Common:1; Rare:65 | ||||
| chr12:79045075-79045307 | Common:3; Rare:80 | ||||
| chr12:79045625-79045661 | Rare:4 | ||||
| chr12:79690481-79690678 | Rare:56 | ||||
| chr12:79690889-79691321 | Common:1; Rare:149 | ||||
| chr12:79691486-79691595 | Rare:27 | ||||
| chr12:79934875-79935396 | Common:1; Rare:194 | ||||
| chr12:80937646-80937875 | Common:1; Rare:70 | ||||
| chr12:81077783-81077881 | Rare:20 |