Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58327227-58327336 | Rare:26 | ||||
chr19:58347508-58347780 | Common:8; Rare:121 | ||||
chr19:58408495-58408686 | Common:2; Rare:58 | ||||
chr19:58440134-58440463 | Common:6; Rare:88 | ||||
chr19:58499216-58499638 | Common:2; Rare:148; Clinvar:6; Clinvar (benign):1 | ||||
chr19:58519767-58519889 | Rare:29 | ||||
chr19:58554046-58554415 | Rare:110 | ||||
chr19:58558957-58559165 | Common:1; Rare:62 | ||||
chr2:264022-264098 | Rare:28 | ||||
chr2:3377833-3378028 | Common:2; Rare:56 | ||||
chr2:3379608-3379779 | Common:2; Rare:72 | ||||
chr2:3519370-3519660 | Common:2; Rare:85 | ||||
chr2:3558225-3558495 | Common:5; Rare:119 | ||||
chr2:3575107-3575358 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
chr2:3594970-3595163 | Rare:75 |