| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56752275-56752535 | Common:1; Rare:76 | ||||
| chr12:57087835-57088088 | Common:1; Rare:66 | ||||
| chr12:57111144-57111440 | Common:4; Rare:56 | ||||
| chr12:57111774-57111903 | Common:1; Rare:28 | ||||
| chr12:57128295-57128499 | Common:1; Rare:46 | ||||
| chr12:57229649-57229781 | Common:1; Rare:66 | ||||
| chr12:57230007-57230194 | Rare:39 | ||||
| chr12:57240702-57240907 | Rare:34 | ||||
| chr12:57430743-57431086 | Common:1; Rare:89 | ||||
| chr12:57455101-57455314 | Rare:35 | ||||
| chr12:57459468-57459878 | Common:4; Rare:77 | ||||
| chr12:57459890-57459908 | Rare:2 | ||||
| chr12:57514748-57515065 | Rare:93; Clinvar:5; Clinvar (benign):2 | ||||
| chr12:57520463-57520725 | Common:2; Rare:84 | ||||
| chr12:57547029-57547214 | Common:1; Rare:49 |