Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:10333500-10333712 | Rare:71 | ||||
chr19:10403475-10403695 | Rare:109 | ||||
chr19:10928651-10928750 | Rare:23 | ||||
chr19:10960689-10961059 | Common:3; Rare:146 | ||||
chr19:11089275-11089516 | Rare:40; Clinvar:9; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr19:11197510-11197654 | Common:1; Rare:45 | ||||
chr19:11529120-11529327 | Common:1; Rare:39 | ||||
chr19:11559195-11559444 | Common:3; Rare:77 | ||||
chr19:11738900-11739252 | Common:4; Rare:92 | ||||
chr19:12156714-12156957 | Common:2; Rare:49 | ||||
chr19:12551461-12551643 | Common:2; Rare:50 | ||||
chr19:12610723-12610947 | Rare:78 | ||||
chr19:12666696-12666809 | Rare:47; Clinvar:4 | ||||
chr19:12696619-12696697 | Rare:36 | ||||
chr19:12722651-12722791 | Rare:25 |