Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48170271-48170699 | Common:2; Rare:115 | ||||
chr19:48363913-48364034 | Common:2; Rare:42 | ||||
chr19:48445909-48446002 | Rare:37 | ||||
chr19:48619144-48619654 | Common:1; Rare:164 | ||||
chr19:48993245-48993474 | Common:2; Rare:111; Clinvar:3; Clinvar (benign):2 | ||||
chr19:49157485-49157780 | Common:2; Rare:81; Clinvar:1 | ||||
chr19:49453094-49453311 | Common:1; Rare:69 | ||||
chr19:49580533-49580623 | Rare:31 | ||||
chr19:49639962-49640498 | Common:1; Rare:168; Clinvar:3; Clinvar (benign):1 | ||||
chr19:49665756-49666020 | Common:3; Rare:128; Clinvar (pathogenic):1 | ||||
chr19:49801594-49801761 | Common:1; Rare:51 | ||||
chr19:49851068-49851182 | Common:1; Rare:45 | ||||
chr19:49877278-49877743 | Common:1; Rare:126 | ||||
chr19:49877867-49878179 | Common:3; Rare:102 | ||||
chr19:49878304-49878535 | Rare:51 |