Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48646168-48646461 | Common:1; Rare:62 | ||||
chr19:48811003-48811126 | Rare:43 | ||||
chr19:48954581-48954916 | Common:1; Rare:115 | ||||
chr19:48965009-48965340 | Common:1; Rare:83 | ||||
chr19:48965342-48965609 | Rare:83; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):6 | ||||
chr19:48993245-48993508 | Common:2; Rare:120; Clinvar:3; Clinvar (benign):2 | ||||
chr19:49114084-49114376 | Common:3; Rare:70 | ||||
chr19:49155388-49155529 | Rare:24 | ||||
chr19:49157666-49157850 | Rare:57; Clinvar:1 | ||||
chr19:49335261-49335413 | Rare:22 | ||||
chr19:49362375-49362525 | Rare:43 | ||||
chr19:49451745-49451851 | Common:1; Rare:27 | ||||
chr19:49453094-49453300 | Common:1; Rare:65 | ||||
chr19:49513716-49514100 | Common:6; Rare:100 | ||||
chr19:49580515-49580620 | Rare:39 |