| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57694573-57694834 | Rare:61 | ||||
| chr12:57744795-57745089 | Common:1; Rare:63 | ||||
| chr12:57772079-57772260 | Rare:62 | ||||
| chr12:57772575-57772670 | Common:3; Rare:12 | ||||
| chr12:57846926-57847221 | Common:2; Rare:109 | ||||
| chr12:57941292-57941561 | Common:5; Rare:84 | ||||
| chr12:59595945-59596196 | Common:5; Rare:62 | ||||
| chr12:62191708-62191872 | Rare:31 | ||||
| chr12:62260165-62260460 | Common:1; Rare:110 | ||||
| chr12:62466607-62466854 | Rare:74 | ||||
| chr12:64222242-64222321 | Rare:28 | ||||
| chr12:64452074-64452174 | Common:1; Rare:35 | ||||
| chr12:64759297-64759496 | Common:1; Rare:62; Clinvar:4 | ||||
| chr12:65169467-65169617 | Common:1; Rare:54; Clinvar:2 | ||||
| chr12:65278437-65278779 | Common:3; Rare:106; Clinvar (benign):1 |