| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:9065054-9065204 | Rare:15 | ||||
| chr12:9072357-9072874 | Rare:119 | ||||
| chr12:29317846-29318088 | Rare:42 | ||||
| chr12:48139574-48139891 | Rare:49 | ||||
| chr12:49565142-49565391 | Common:2; Rare:50 | ||||
| chr12:55688052-55688181 | Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:55703575-55703668 | Rare:9 | ||||
| chr12:55709852-55710158 | Common:5; Rare:58 | ||||
| chr12:57803657-57803785 | Rare:33 | ||||
| chr12:70550012-70550322 | Common:3; Rare:53 | ||||
| chr12:98503843-98504050 | Common:3; Rare:57 | ||||
| chr12:101761223-101761490 | Rare:57; Clinvar (pathogenic):2 | ||||
| chr12:109222613-109222879 | Common:4; Rare:81 | ||||
| chr12:110339278-110339721 | Rare:83; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:123084074-123084354 | Common:2; Rare:36 |