| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49527761-49528033 | Common:4; Rare:85 | ||||
| chr19:49580515-49580692 | Rare:58 | ||||
| chr19:49665747-49666025 | Common:3; Rare:133; Clinvar (pathogenic):1 | ||||
| chr19:49877277-49877717 | Common:1; Rare:111 | ||||
| chr19:49877876-49878193 | Common:3; Rare:103 | ||||
| chr19:49929451-49929820 | Common:7; Rare:128 | ||||
| chr19:49929922-49930219 | Common:1; Rare:71 | ||||
| chr19:50476358-50476547 | Rare:89 | ||||
| chr19:50804590-50804913 | Common:6; Rare:97 | ||||
| chr19:51366325-51366551 | Common:5; Rare:64; Clinvar (benign):2 | ||||
| chr19:52028336-52028503 | Common:3; Rare:33 | ||||
| chr19:52397719-52397890 | Common:5; Rare:52 | ||||
| chr19:52735016-52735178 | Common:4; Rare:44 | ||||
| chr19:53254808-53255079 | Common:3; Rare:98 | ||||
| chr19:53867583-53867943 | Common:1; Rare:88 |