Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:9827814-9827948 | Common:1; Rare:49 | ||||
chr19:9835034-9835340 | Rare:127 | ||||
chr19:10116873-10117149 | Rare:78 | ||||
chr19:10315743-10316031 | Common:6; Rare:129; Clinvar (benign):10 | ||||
chr19:10333481-10333715 | Common:1; Rare:82 | ||||
chr19:10380487-10380824 | Common:12; Rare:98; Clinvar:5 | ||||
chr19:10502696-10502925 | Rare:62 | ||||
chr19:10653814-10653881 | Rare:28 | ||||
chr19:10836271-10836551 | Common:2; Rare:71 | ||||
chr19:10928517-10928811 | Common:2; Rare:86 | ||||
chr19:10960708-10961058 | Common:3; Rare:137 | ||||
chr19:11089364-11089516 | Rare:27; Clinvar:5; Clinvar (pathogenic):1 | ||||
chr19:11197504-11197687 | Common:1; Rare:59 | ||||
chr19:11197820-11197979 | Rare:50 | ||||
chr19:11355377-11355486 | Common:1; Rare:47 |