| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57240724-57240775 | Rare:6 | ||||
| chr12:57533991-57534310 | Rare:86 | ||||
| chr12:57549789-57550128 | Rare:77 | ||||
| chr12:57550228-57550559 | Common:1; Rare:77; Clinvar (benign):2 | ||||
| chr12:57604572-57604857 | Rare:52 | ||||
| chr12:57611214-57611480 | Rare:55 | ||||
| chr12:57632495-57632810 | Common:1; Rare:64 | ||||
| chr12:57633101-57633277 | Rare:54 | ||||
| chr12:57731605-57731933 | Common:1; Rare:88 | ||||
| chr12:57744827-57745089 | Common:1; Rare:58 | ||||
| chr12:57745248-57745422 | Common:1; Rare:39 | ||||
| chr12:57752241-57752657 | Rare:112; Clinvar:1 | ||||
| chr12:57772087-57772293 | Rare:62 | ||||
| chr12:57941360-57941688 | Common:3; Rare:96 | ||||
| chr12:58920128-58920308 | Common:1; Rare:55 |