| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49580534-49580674 | Rare:45 | ||||
| chr19:49639953-49640061 | Rare:37; Clinvar:3 | ||||
| chr19:49640074-49640405 | Common:1; Rare:102 | ||||
| chr19:49665853-49666019 | Common:2; Rare:85; Clinvar (pathogenic):1 | ||||
| chr19:49877278-49877710 | Common:1; Rare:107 | ||||
| chr19:49878032-49878141 | Common:1; Rare:33 | ||||
| chr19:49878317-49878491 | Rare:32 | ||||
| chr19:49929096-49929224 | Common:3; Rare:38 | ||||
| chr19:49929427-49929832 | Common:7; Rare:140 | ||||
| chr19:50476409-50476558 | Rare:67 | ||||
| chr19:50804590-50804909 | Common:6; Rare:96 | ||||
| chr19:52397707-52397880 | Common:3; Rare:52 | ||||
| chr19:53254815-53255024 | Common:1; Rare:68 | ||||
| chr19:54115270-54115425 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chr19:54115627-54115790 | Common:1; Rare:39; Clinvar:4 |