Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:9793150-9793370 | Rare:44 | ||||
chr19:9818800-9818851 | Rare:14 | ||||
chr19:9827838-9827974 | Common:1; Rare:50 | ||||
chr19:10333512-10333701 | Rare:63 | ||||
chr19:10353605-10353710 | Rare:30; Clinvar (pathogenic):1 | ||||
chr19:10928578-10928781 | Common:1; Rare:52 | ||||
chr19:11196125-11196423 | Rare:73 | ||||
chr19:11197504-11197644 | Common:1; Rare:43 | ||||
chr19:11197753-11197979 | Common:2; Rare:66 | ||||
chr19:11203425-11203766 | Rare:81 | ||||
chr19:11419279-11419440 | Common:1; Rare:33 | ||||
chr19:11559195-11559407 | Common:1; Rare:66 | ||||
chr19:11848620-11848773 | Common:1; Rare:43 | ||||
chr19:11887691-11887844 | Common:1; Rare:42 | ||||
chr19:11964923-11965068 | Common:1; Rare:38 |