| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57772092-57772229 | Rare:50 | ||||
| chr12:62260033-62260495 | Common:1; Rare:170 | ||||
| chr12:62305742-62305919 | Rare:34 | ||||
| chr12:64452080-64452174 | Common:1; Rare:33 | ||||
| chr12:64759357-64759667 | Common:3; Rare:92; Clinvar:3 | ||||
| chr12:66130700-66130861 | Rare:57 | ||||
| chr12:66169921-66170112 | Common:1; Rare:57 | ||||
| chr12:68807859-68808234 | Common:3; Rare:107 | ||||
| chr12:69239418-69239656 | Common:2; Rare:98 | ||||
| chr12:69348323-69348568 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:70338456-70338758 | Rare:70 | ||||
| chr12:71662793-71662987 | Rare:48 | ||||
| chr12:71663033-71663065 | Rare:5 | ||||
| chr12:71663718-71663908 | Common:1; Rare:56 | ||||
| chr12:74537707-74537871 | Common:1; Rare:61 |