Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:47484173-47484299 | Common:2; Rare:42 | ||||
chr19:48170273-48170705 | Common:2; Rare:116 | ||||
chr19:48445890-48446005 | Rare:44 | ||||
chr19:48619144-48619654 | Common:1; Rare:164 | ||||
chr19:48811005-48811191 | Rare:56 | ||||
chr19:48993301-48993580 | Common:2; Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
chr19:49453094-49453311 | Common:1; Rare:69 | ||||
chr19:49527858-49528031 | Common:3; Rare:55 | ||||
chr19:49640087-49640485 | Common:1; Rare:120 | ||||
chr19:49665734-49666035 | Common:3; Rare:140; Clinvar (pathogenic):1 | ||||
chr19:49851064-49851167 | Rare:39 | ||||
chr19:49877255-49877726 | Common:2; Rare:118 | ||||
chr19:49929404-49929811 | Common:7; Rare:137 | ||||
chr19:50511084-50511548 | Common:4; Rare:150 | ||||
chr19:51366273-51366588 | Common:8; Rare:98; Clinvar (benign):2 |