| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57771724-57771961 | Rare:71 | ||||
| chr12:57772035-57772380 | Common:1; Rare:213 | ||||
| chr12:57772446-57772755 | Common:9; Rare:101 | ||||
| chr12:57782708-57782883 | Common:2; Rare:74; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:57816968-57817233 | Rare:55 | ||||
| chr12:57845520-57845887 | Common:9; Rare:213 | ||||
| chr12:57846310-57846590 | Common:1; Rare:128 | ||||
| chr12:57846545-57846835 | Common:3; Rare:169 | ||||
| chr12:57846881-57847265 | Common:8; Rare:375 | ||||
| chr12:57941095-57941793 | Common:13; Rare:390 | ||||
| chr12:58920146-58920830 | Common:12; Rare:502 | ||||
| chr12:59595771-59596212 | Common:14; Rare:181 | ||||
| chr12:59596268-59596612 | Common:9; Rare:103 | ||||
| chr12:59596923-59597191 | Common:2; Rare:104 | ||||
| chr12:59597543-59597773 | Common:1; Rare:37 |