| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57203168-57203518 | Common:1; Rare:103 | ||||
| chr12:57479595-57479637 | Rare:5 | ||||
| chr12:57520467-57520737 | Common:2; Rare:84 | ||||
| chr12:57772079-57772215 | Rare:52 | ||||
| chr12:57772524-57772626 | Common:2; Rare:13 | ||||
| chr12:57941292-57941688 | Common:5; Rare:114 | ||||
| chr12:58920491-58920657 | Common:2; Rare:58 | ||||
| chr12:59595915-59596175 | Common:5; Rare:64 | ||||
| chr12:62260056-62260445 | Common:1; Rare:147 | ||||
| chr12:63844781-63844828 | Common:1; Rare:17 | ||||
| chr12:64222242-64222346 | Rare:35 | ||||
| chr12:64452043-64452174 | Common:1; Rare:47 | ||||
| chr12:64759115-64759467 | Rare:111; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:64780695-64780811 | Rare:27 | ||||
| chr12:65169480-65169599 | Common:1; Rare:41; Clinvar:1 |