| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47094339-47094437 | Rare:15 | ||||
| chr12:47135254-47135272 | Rare:1 | ||||
| chr12:47142372-47142541 | Rare:26 | ||||
| chr12:47267633-47267898 | Rare:44 | ||||
| chr12:47276665-47276856 | Rare:30 | ||||
| chr12:48085371-48085570 | Rare:39 | ||||
| chr12:48643558-48643775 | Rare:36 | ||||
| chr12:48697573-48697835 | Common:1; Rare:29 | ||||
| chr12:48787225-48787522 | Rare:60 | ||||
| chr12:48927336-48927526 | Rare:37 | ||||
| chr12:48928290-48928329 | Rare:11 | ||||
| chr12:49041962-49042116 | Common:2; Rare:49; Clinvar (pathogenic):1 | ||||
| chr12:49511540-49511718 | Rare:29 | ||||
| chr12:49635107-49635424 | Rare:91 | ||||
| chr12:50086643-50086841 | Rare:49 |