Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44356645-44356842 | Common:1; Rare:41 | ||||
chr19:44500494-44500650 | Common:3; Rare:46 | ||||
chr19:44643803-44644028 | Rare:56 | ||||
chr19:44757423-44757580 | Rare:35 | ||||
chr19:44954924-44955017 | Common:2; Rare:26 | ||||
chr19:45079058-45079296 | Common:1; Rare:59 | ||||
chr19:45091591-45091792 | Common:1; Rare:52 | ||||
chr19:45370552-45370791 | Common:2; Rare:70 | ||||
chr19:45406339-45406694 | Common:3; Rare:90 | ||||
chr19:45423502-45423790 | Common:2; Rare:60; Clinvar (benign):1 | ||||
chr19:45496949-45497271 | Common:2; Rare:97 | ||||
chr19:45507229-45507641 | Common:1; Rare:110 | ||||
chr19:45639372-45639478 | Rare:33 | ||||
chr19:45692373-45692708 | Common:1; Rare:78 | ||||
chr19:45770549-45770923 | Common:4; Rare:162; Clinvar:1 |