Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48619139-48619435 | Rare:96 | ||||
chr19:48964986-48965359 | Common:1; Rare:89; Clinvar (pathogenic):4 | ||||
chr19:48965670-48965916 | Common:1; Rare:94; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr19:48993296-48993510 | Common:1; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
chr19:49114074-49114434 | Common:4; Rare:96 | ||||
chr19:49119093-49119275 | Rare:55 | ||||
chr19:49453094-49453324 | Common:1; Rare:71 | ||||
chr19:49580534-49580717 | Common:1; Rare:51 | ||||
chr19:49665784-49665931 | Rare:71; Clinvar (pathogenic):1 | ||||
chr19:49851083-49851124 | Rare:17 | ||||
chr19:49877268-49877742 | Common:2; Rare:125 | ||||
chr19:49877899-49878157 | Common:2; Rare:82 | ||||
chr19:49929451-49929785 | Common:7; Rare:112 | ||||
chr19:50377603-50377794 | Rare:72 | ||||
chr19:50476234-50476547 | Common:1; Rare:146 |