| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57579779-57580002 | Rare:42 | ||||
| chr12:57726146-57726325 | Rare:45 | ||||
| chr12:57747206-57747289 | Rare:18 | ||||
| chr12:57764677-57764937 | Common:1; Rare:78; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:57844798-57844959 | Rare:37 | ||||
| chr12:57865161-57865260 | Common:1; Rare:19 | ||||
| chr12:57865312-57865559 | Rare:55 | ||||
| chr12:57865621-57865684 | Rare:14 | ||||
| chr12:57936046-57936299 | Common:3; Rare:66 | ||||
| chr12:58364931-58365125 | Common:1; Rare:27 | ||||
| chr12:58413828-58414176 | Common:4; Rare:54 | ||||
| chr12:58414670-58414865 | Common:4; Rare:33 | ||||
| chr12:58425480-58425709 | Common:3; Rare:33 | ||||
| chr12:58426167-58426277 | Rare:27 | ||||
| chr12:58766011-58766265 | Common:1; Rare:40 |