Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:10960689-10961141 | Common:3; Rare:168; Clinvar (benign):1 | ||||
chr19:11090334-11090579 | Common:2; Rare:64 | ||||
chr19:11170329-11170610 | Common:1; Rare:60 | ||||
chr19:11197483-11197676 | Common:1; Rare:59 | ||||
chr19:11203408-11203779 | Rare:90 | ||||
chr19:11374941-11375239 | Common:1; Rare:69 | ||||
chr19:11419287-11419433 | Rare:32 | ||||
chr19:11435190-11435443 | Common:2; Rare:67 | ||||
chr19:11435534-11435705 | Common:3; Rare:67; Clinvar:2; Clinvar (benign):3 | ||||
chr19:11529073-11529414 | Common:3; Rare:63 | ||||
chr19:11538674-11538988 | Common:3; Rare:76 | ||||
chr19:11539755-11540095 | Common:2; Rare:73 | ||||
chr19:11540151-11540574 | Common:3; Rare:80 | ||||
chr19:11546661-11546969 | Rare:83 | ||||
chr19:11559190-11559391 | Common:1; Rare:63 |