| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49665725-49666020 | Common:3; Rare:136; Clinvar (pathogenic):1 | ||||
| chr19:49808827-49808933 | Rare:39 | ||||
| chr19:49850990-49851024 | Rare:13 | ||||
| chr19:49851067-49851120 | Rare:21 | ||||
| chr19:49854502-49854717 | Common:1; Rare:82 | ||||
| chr19:49857589-49857779 | Common:2; Rare:81 | ||||
| chr19:49867509-49867620 | Common:2; Rare:36; Clinvar:1 | ||||
| chr19:49877049-49877149 | Rare:18 | ||||
| chr19:49877264-49877742 | Common:2; Rare:125 | ||||
| chr19:49877913-49878190 | Common:2; Rare:92 | ||||
| chr19:49928630-49928909 | Common:1; Rare:61 | ||||
| chr19:49929408-49929820 | Common:7; Rare:140 | ||||
| chr19:49929923-49930219 | Common:1; Rare:70 | ||||
| chr19:50476240-50476544 | Rare:141 | ||||
| chr19:50511137-50511276 | Rare:49 |