| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57941360-57941707 | Common:3; Rare:102 | ||||
| chr12:59595895-59596209 | Common:5; Rare:72 | ||||
| chr12:62260059-62260460 | Common:1; Rare:149 | ||||
| chr12:62466614-62466908 | Rare:83 | ||||
| chr12:63779760-63780175 | Common:3; Rare:167; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr12:64222223-64222396 | Common:1; Rare:60 | ||||
| chr12:64404221-64404804 | Common:5; Rare:196 | ||||
| chr12:64404940-64405117 | Rare:41 | ||||
| chr12:64452001-64452366 | Common:1; Rare:126 | ||||
| chr12:64759364-64759683 | Common:3; Rare:93; Clinvar:3 | ||||
| chr12:65169456-65169602 | Common:1; Rare:48; Clinvar:1 | ||||
| chr12:65278646-65278756 | Rare:34 | ||||
| chr12:66130683-66130924 | Rare:73 | ||||
| chr12:66169921-66170127 | Common:1; Rare:62 | ||||
| chr12:67269138-67269706 | Common:4; Rare:176 |