| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:15882225-15882666 | Common:1; Rare:145 | ||||
| chr12:16606420-16606677 | Rare:61 | ||||
| chr12:19129554-19129886 | Common:2; Rare:149 | ||||
| chr12:19130549-19130785 | Rare:59 | ||||
| chr12:19205383-19205414 | Rare:5 | ||||
| chr12:19236781-19236947 | Rare:39 | ||||
| chr12:19439336-19439745 | Common:3; Rare:151 | ||||
| chr12:21437487-21437717 | Common:7; Rare:76 | ||||
| chr12:21501516-21501915 | Common:6; Rare:114 | ||||
| chr12:21657753-21657997 | Common:4; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:22333580-22333844 | Rare:59 | ||||
| chr12:22334669-22335045 | Common:1; Rare:113 | ||||
| chr12:22544132-22544292 | Common:1; Rare:74 | ||||
| chr12:22544448-22544701 | Common:2; Rare:60 | ||||
| chr12:22625034-22625257 | Rare:117 |