Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:38831774-38832045 | Common:3; Rare:77 | ||||
chr19:38899528-38900018 | Rare:149 | ||||
chr19:38930742-38930996 | Common:3; Rare:67; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39391025-39391418 | Common:1; Rare:158 | ||||
chr19:39435893-39436167 | Common:5; Rare:104 | ||||
chr19:39445476-39445802 | Common:2; Rare:88 | ||||
chr19:39480716-39480912 | Common:3; Rare:106; Clinvar (pathogenic):1 | ||||
chr19:39846306-39846477 | Common:1; Rare:80 | ||||
chr19:39970969-39971216 | Common:2; Rare:67 | ||||
chr19:40056166-40056342 | Rare:32 | ||||
chr19:40090886-40090989 | Common:1; Rare:28 | ||||
chr19:40285243-40285623 | Common:3; Rare:131 | ||||
chr19:40348388-40348731 | Common:4; Rare:113 | ||||
chr19:40425987-40426134 | Common:1; Rare:42 | ||||
chr19:40751076-40751220 | Common:1; Rare:35 |