| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:14567685-14567970 | Common:2; Rare:60 | ||||
| chr12:14771091-14771244 | Common:1; Rare:63 | ||||
| chr12:14774184-14774477 | Common:3; Rare:76 | ||||
| chr12:14803439-14803759 | Common:1; Rare:88 | ||||
| chr12:14885732-14885940 | Common:3; Rare:43; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:15221244-15221547 | Common:1; Rare:85 | ||||
| chr12:15789145-15789549 | Common:1; Rare:120 | ||||
| chr12:15882219-15882621 | Common:1; Rare:130 | ||||
| chr12:15911252-15911392 | Common:5; Rare:55 | ||||
| chr12:19129425-19129825 | Common:3; Rare:167 | ||||
| chr12:20369558-20369908 | Common:3; Rare:158 | ||||
| chr12:21501556-21501880 | Common:2; Rare:84 | ||||
| chr12:21657766-21657978 | Common:4; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:21941203-21941326 | Rare:23 | ||||
| chr12:21941360-21941630 | Common:1; Rare:46 |