Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:20982167-20982532 | Common:2; Rare:112; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
chr22:21002088-21002273 | Common:5; Rare:69 | ||||
chr22:21642055-21642346 | Common:2; Rare:87 | ||||
chr22:21665924-21666100 | Common:1; Rare:56 | ||||
chr22:21867327-21867853 | Common:5; Rare:148 | ||||
chr22:21982718-21982903 | Rare:51 | ||||
chr22:22508704-22508855 | Rare:51 | ||||
chr22:23145173-23145551 | Common:3; Rare:124 | ||||
chr22:23750974-23751198 | Common:1; Rare:77 | ||||
chr22:23786874-23787126 | Common:2; Rare:90; Clinvar:4; Clinvar (benign):2 | ||||
chr22:23857065-23857225 | Common:8; Rare:52 | ||||
chr22:23857525-23857933 | Common:7; Rare:174 | ||||
chr22:23858128-23858458 | Common:2; Rare:70 | ||||
chr22:23894166-23894526 | Common:5; Rare:125 | ||||
chr22:23894575-23894804 | Common:3; Rare:85 |