Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58347599-58347786 | Common:8; Rare:90 | ||||
chr19:58393106-58393435 | Common:3; Rare:86 | ||||
chr19:58408452-58408623 | Common:2; Rare:51 | ||||
chr19:58499206-58499549 | Common:2; Rare:114; Clinvar:5; Clinvar (benign):1 | ||||
chr19:58519617-58519870 | Rare:54 | ||||
chr19:58549608-58549792 | Rare:52 | ||||
chr19:58558377-58558688 | Rare:99 | ||||
chr19:58558956-58559132 | Common:1; Rare:50 | ||||
chr19:58573298-58573505 | Rare:51 | ||||
chr2:3519516-3519635 | Common:1; Rare:34 | ||||
chr2:3558256-3558676 | Common:6; Rare:153 | ||||
chr2:3575107-3575354 | Common:2; Rare:72; Clinvar:3; Clinvar (benign):5 | ||||
chr2:6865470-6865822 | Common:1; Rare:103 | ||||
chr2:8837590-8837778 | Common:1; Rare:67 | ||||
chr2:9423148-9423296 | Common:1; Rare:30 |