| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57111127-57111447 | Common:4; Rare:59 | ||||
| chr12:57111792-57111903 | Common:1; Rare:22 | ||||
| chr12:57128295-57128493 | Common:1; Rare:45 | ||||
| chr12:57128607-57128897 | Rare:58 | ||||
| chr12:57201514-57201794 | Common:2; Rare:66 | ||||
| chr12:57229659-57229796 | Common:1; Rare:63 | ||||
| chr12:57230731-57230862 | Rare:41 | ||||
| chr12:57431153-57431209 | Common:2; Rare:26 | ||||
| chr12:57489956-57490274 | Common:2; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:57520501-57520729 | Common:1; Rare:68 | ||||
| chr12:57522948-57522978 | Rare:4 | ||||
| chr12:57524475-57524747 | Rare:74 | ||||
| chr12:57527743-57527930 | Rare:57 | ||||
| chr12:57716088-57716732 | Common:4; Rare:166 | ||||
| chr12:57720281-57720497 | Rare:71 |