| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46383584-46383703 | Common:2; Rare:28 | ||||
| chr12:47080797-47080948 | Common:1; Rare:48 | ||||
| chr12:50106810-50107156 | Rare:100 | ||||
| chr12:50107763-50108045 | Rare:83; Clinvar (pathogenic):1 | ||||
| chr12:53027540-53027805 | Common:1; Rare:65 | ||||
| chr12:53027807-53028185 | Common:1; Rare:129 | ||||
| chr12:53039158-53039318 | Common:3; Rare:38 | ||||
| chr12:55697215-55697477 | Common:2; Rare:70; Clinvar (benign):3 | ||||
| chr12:55703170-55703302 | Common:1; Rare:34 | ||||
| chr12:55709683-55709985 | Common:2; Rare:46 | ||||
| chr12:55834901-55834977 | Common:1; Rare:12 | ||||
| chr12:55981041-55981148 | Rare:29 | ||||
| chr12:57162766-57162982 | Rare:56 | ||||
| chr12:57165790-57166136 | Common:1; Rare:83 | ||||
| chr12:57179616-57180102 | Rare:125 |