Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48619139-48619242 | Rare:49 | ||||
chr19:48993294-48993533 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):1 | ||||
chr19:48993749-48993907 | Common:4; Rare:51 | ||||
chr19:49453473-49453639 | Common:1; Rare:48 | ||||
chr19:49665765-49666038 | Common:2; Rare:133; Clinvar (pathogenic):1 | ||||
chr19:49867531-49867689 | Common:3; Rare:44 | ||||
chr19:49877333-49877697 | Common:1; Rare:89 | ||||
chr19:50384013-50384311 | Common:3; Rare:127 | ||||
chr19:50384326-50384367 | Rare:14; Clinvar (benign):2 | ||||
chr19:50476336-50476539 | Rare:88 | ||||
chr19:50969553-50969870 | Rare:78 | ||||
chr19:51019702-51020013 | Common:5; Rare:55 | ||||
chr19:51026567-51026781 | Common:2; Rare:59 | ||||
chr19:54115628-54115797 | Common:1; Rare:43; Clinvar:4 | ||||
chr19:54200658-54200901 | Common:4; Rare:93 |