Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49155360-49155528 | Rare:27 | ||||
chr19:49335387-49335490 | Common:1; Rare:24 | ||||
chr19:49362367-49362473 | Rare:27 | ||||
chr19:49451756-49452022 | Common:3; Rare:75 | ||||
chr19:49453094-49453313 | Common:1; Rare:70 | ||||
chr19:49453459-49453612 | Rare:48 | ||||
chr19:49496363-49496470 | Common:1; Rare:55 | ||||
chr19:49513087-49513405 | Common:1; Rare:71 | ||||
chr19:49513747-49514045 | Common:3; Rare:71 | ||||
chr19:49580528-49580686 | Rare:51 | ||||
chr19:49665738-49666038 | Common:3; Rare:139; Clinvar (pathogenic):1 | ||||
chr19:49690980-49691138 | Rare:36 | ||||
chr19:49808613-49808981 | Common:2; Rare:134; Clinvar:1 | ||||
chr19:49851075-49851167 | Rare:33 | ||||
chr19:49877264-49877742 | Common:2; Rare:125 |