| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48619139-48619435 | Rare:96 | ||||
| chr19:48872218-48872427 | Common:2; Rare:64 | ||||
| chr19:48954724-48954922 | Rare:71 | ||||
| chr19:48965691-48965850 | Common:1; Rare:61; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:48993290-48993485 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:49085093-49085522 | Common:3; Rare:170 | ||||
| chr19:49527880-49528024 | Common:3; Rare:40 | ||||
| chr19:49580534-49580681 | Rare:45 | ||||
| chr19:49665784-49666027 | Common:2; Rare:129; Clinvar (pathogenic):1 | ||||
| chr19:49929923-49930219 | Common:1; Rare:70 | ||||
| chr19:50476226-50476538 | Common:1; Rare:145 | ||||
| chr19:51366333-51366595 | Common:8; Rare:74; Clinvar (benign):2 | ||||
| chr19:52028373-52028456 | Common:2; Rare:13 | ||||
| chr19:52492640-52492836 | Common:4; Rare:65 | ||||
| chr19:53333575-53333768 | Common:3; Rare:60 |