Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48619139-48619428 | Rare:92 | ||||
chr19:48872218-48872427 | Common:2; Rare:64 | ||||
chr19:48965242-48965609 | Rare:114; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
chr19:48993211-48993584 | Common:4; Rare:162; Clinvar:3; Clinvar (benign):3 | ||||
chr19:49085123-49085492 | Common:3; Rare:148 | ||||
chr19:49451754-49452002 | Common:3; Rare:64 | ||||
chr19:49453024-49453311 | Common:2; Rare:88 | ||||
chr19:49527864-49528038 | Common:3; Rare:53 | ||||
chr19:49580528-49580680 | Rare:49 | ||||
chr19:49665747-49666029 | Common:3; Rare:136; Clinvar (pathogenic):1 | ||||
chr19:49813258-49813339 | Rare:34 | ||||
chr19:49817346-49817641 | Common:3; Rare:63 | ||||
chr19:49867518-49867689 | Common:3; Rare:48; Clinvar:1 | ||||
chr19:49877319-49877726 | Common:1; Rare:105 | ||||
chr19:49877836-49878161 | Common:5; Rare:102 |