Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:19033467-19033658 | Common:2; Rare:63 | ||||
chr19:19033820-19033914 | Common:1; Rare:25 | ||||
chr19:19192124-19192259 | Common:1; Rare:41 | ||||
chr19:19192596-19192996 | Common:3; Rare:100; Clinvar (benign):1 | ||||
chr19:19320485-19320851 | Common:4; Rare:129 | ||||
chr19:19516163-19516287 | Rare:77; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr19:19821700-19821873 | Common:1; Rare:58 | ||||
chr19:19900762-19900977 | Common:1; Rare:61 | ||||
chr19:21396967-21397140 | Rare:37 | ||||
chr19:29213138-29213303 | Common:3; Rare:54 | ||||
chr19:29665252-29665524 | Common:4; Rare:100 | ||||
chr19:29715192-29715325 | Common:1; Rare:55 | ||||
chr19:32405551-32405835 | Common:1; Rare:120 | ||||
chr19:32406033-32406188 | Rare:47 | ||||
chr19:32675133-32675407 | Common:3; Rare:92 |