Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:33402437-33402607 | Common:2; Rare:31 | ||||
chr19:33402695-33402860 | Rare:38 | ||||
chr19:34173422-34173494 | Rare:11 | ||||
chr19:34381413-34381515 | Common:2; Rare:31; Clinvar (benign):1 | ||||
chr19:34399071-34399335 | Common:1; Rare:61; Clinvar (pathogenic):1 | ||||
chr19:35060507-35060672 | Common:2; Rare:53 | ||||
chr19:35065543-35066042 | Common:7; Rare:119 | ||||
chr19:35137003-35137229 | Rare:30 | ||||
chr19:36142526-36142720 | Common:1; Rare:60 | ||||
chr19:36142725-36142953 | Rare:53 | ||||
chr19:39974347-39974582 | Common:2; Rare:69 | ||||
chr19:40608313-40608592 | Common:2; Rare:101; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr19:40823808-40824110 | Common:2; Rare:61 | ||||
chr19:42287190-42287447 | Common:1; Rare:84; Clinvar:2 | ||||
chr19:44725166-44725455 | Common:5; Rare:72 |