| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:28162585-28162738 | Rare:21 | ||||
| chr12:28244542-28244613 | Rare:9 | ||||
| chr12:28248162-28248474 | Common:2; Rare:59 | ||||
| chr12:28248791-28248950 | Common:1; Rare:21 | ||||
| chr12:28254523-28254764 | Rare:48 | ||||
| chr12:28260856-28261002 | Rare:29 | ||||
| chr12:28375931-28376100 | Common:2; Rare:32 | ||||
| chr12:29744042-29744130 | Common:1; Rare:18 | ||||
| chr12:30649140-30649386 | Rare:50 | ||||
| chr12:30795908-30796207 | Common:1; Rare:72 | ||||
| chr12:32350530-32350626 | Common:1; Rare:9 | ||||
| chr12:32585045-32585302 | Common:2; Rare:47 | ||||
| chr12:32585460-32585509 | Rare:8 | ||||
| chr12:32597826-32597852 | Rare:4 | ||||
| chr12:32598274-32598590 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |