| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2890727-2890948 | Common:1; Rare:83 | ||||
| chr12:4538453-4538933 | Common:3; Rare:108 | ||||
| chr12:4649049-4649149 | Common:1; Rare:42; Clinvar (benign):1 | ||||
| chr12:6451785-6452159 | Common:4; Rare:70 | ||||
| chr12:6493224-6493387 | Common:6; Rare:45 | ||||
| chr12:6534242-6534560 | Common:6; Rare:127 | ||||
| chr12:6568249-6568388 | Rare:53 | ||||
| chr12:6723834-6724182 | Common:1; Rare:78 | ||||
| chr12:6828348-6828416 | Common:2; Rare:8 | ||||
| chr12:6828558-6828857 | Rare:71 | ||||
| chr12:6851238-6851486 | Rare:59 | ||||
| chr12:6970557-6970955 | Common:3; Rare:122 | ||||
| chr12:7108475-7108701 | Common:1; Rare:61 | ||||
| chr12:10172122-10172258 | Rare:32 | ||||
| chr12:11171597-11171708 | Common:1; Rare:35 |