| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57772014-57772251 | Rare:94 | ||||
| chr12:57772506-57772642 | Common:2; Rare:23 | ||||
| chr12:57941552-57941746 | Rare:55 | ||||
| chr12:62260133-62260495 | Common:1; Rare:135 | ||||
| chr12:64222248-64222349 | Rare:33 | ||||
| chr12:64404224-64404720 | Common:5; Rare:174 | ||||
| chr12:64452029-64452183 | Common:1; Rare:56 | ||||
| chr12:64610335-64610608 | Common:4; Rare:94 | ||||
| chr12:64759088-64759504 | Common:1; Rare:130; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:65169460-65169605 | Common:1; Rare:48; Clinvar:1 | ||||
| chr12:65824030-65824268 | Common:1; Rare:54 | ||||
| chr12:65824355-65824755 | Common:7; Rare:133 | ||||
| chr12:65824765-65825379 | Common:1; Rare:145 | ||||
| chr12:66130678-66130889 | Rare:69 | ||||
| chr12:67269140-67269512 | Common:3; Rare:103 |