| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32896368-32896449 | Rare:18 | ||||
| chr12:32896523-32896602 | Common:1; Rare:29; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr12:32896718-32897123 | Common:4; Rare:129; Clinvar:4; Clinvar (benign):7 | ||||
| chr12:32897125-32897361 | Common:1; Rare:56 | ||||
| chr12:34022373-34022589 | Common:2; Rare:65 | ||||
| chr12:38905541-38905797 | Common:5; Rare:71 | ||||
| chr12:38906683-38906891 | Common:1; Rare:45 | ||||
| chr12:39442412-39442747 | Rare:69 | ||||
| chr12:39442988-39443600 | Common:2; Rare:169; Clinvar:9; Clinvar (benign):6 | ||||
| chr12:39443611-39443835 | Rare:52 | ||||
| chr12:40105460-40105474 | Rare:5 | ||||
| chr12:40106013-40106191 | Common:1; Rare:79 | ||||
| chr12:42144221-42144330 | Common:4; Rare:37 | ||||
| chr12:42144414-42144491 | Common:1; Rare:24 | ||||
| chr12:42144547-42145100 | Common:12; Rare:223 |