| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57239128-57239421 | Common:1; Rare:65 | ||||
| chr12:57242731-57242926 | Rare:53 | ||||
| chr12:57249096-57249293 | Rare:54; Clinvar:5; Clinvar (benign):1 | ||||
| chr12:57280341-57280516 | Common:1; Rare:37 | ||||
| chr12:57458971-57459120 | Rare:21 | ||||
| chr12:57459122-57459415 | Common:1; Rare:56 | ||||
| chr12:57462715-57462924 | Common:1; Rare:51 | ||||
| chr12:57477165-57477204 | Rare:11 | ||||
| chr12:57744067-57744368 | Common:2; Rare:52 | ||||
| chr12:57836786-57837117 | Common:2; Rare:62 | ||||
| chr12:57838201-57838487 | Rare:58 | ||||
| chr12:57844457-57844780 | Common:1; Rare:75 | ||||
| chr12:57865148-57865255 | Common:1; Rare:23 | ||||
| chr12:57898513-57898570 | Rare:4 | ||||
| chr12:57936013-57936367 | Common:4; Rare:89 |