| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57716141-57716512 | Common:4; Rare:89 | ||||
| chr12:57744821-57745093 | Common:1; Rare:58 | ||||
| chr12:57751864-57751927 | Rare:9 | ||||
| chr12:57752241-57752587 | Rare:93; Clinvar:1 | ||||
| chr12:57772070-57772293 | Rare:73 | ||||
| chr12:57772493-57772670 | Common:3; Rare:32 | ||||
| chr12:57782632-57782842 | Common:3; Rare:77; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:57846444-57846467 | Rare:8 | ||||
| chr12:57941292-57941699 | Common:5; Rare:118 | ||||
| chr12:59595874-59596190 | Common:5; Rare:75 | ||||
| chr12:62260165-62260423 | Common:1; Rare:92 | ||||
| chr12:62466662-62466854 | Rare:64 | ||||
| chr12:63668459-63668622 | Rare:44 | ||||
| chr12:63668627-63668668 | Rare:13 | ||||
| chr12:63779749-63779917 | Common:2; Rare:58 |