| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56609851-56610182 | Common:1; Rare:90 | ||||
| chr12:56645931-56646283 | Common:1; Rare:90 | ||||
| chr12:56688236-56688567 | Common:3; Rare:119 | ||||
| chr12:56724934-56725094 | Rare:28 | ||||
| chr12:56752309-56752505 | Rare:58 | ||||
| chr12:57110505-57110621 | Rare:22 | ||||
| chr12:57111150-57111444 | Common:4; Rare:55 | ||||
| chr12:57111802-57111903 | Common:1; Rare:19 | ||||
| chr12:57128348-57128906 | Common:1; Rare:108 | ||||
| chr12:57240703-57240866 | Rare:27 | ||||
| chr12:57430722-57431116 | Common:2; Rare:102 | ||||
| chr12:57488791-57489109 | Common:3; Rare:75; Clinvar (benign):2 | ||||
| chr12:57534031-57534309 | Rare:73 | ||||
| chr12:57694198-57694319 | Common:1; Rare:27 | ||||
| chr12:57716407-57716725 | Rare:91 |