Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:19854811-19855006 | Rare:71 | ||||
chr22:19941719-19941878 | Rare:69; Clinvar:5; Clinvar (benign):4 | ||||
chr22:20020911-20021141 | Common:1; Rare:73 | ||||
chr22:20079921-20080247 | Common:1; Rare:102 | ||||
chr22:20117175-20117571 | Common:3; Rare:127 | ||||
chr22:20319994-20320166 | Common:2; Rare:58 | ||||
chr22:20495787-20495919 | Common:1; Rare:50 | ||||
chr22:20858704-20859105 | Common:7; Rare:203; Clinvar:3; Clinvar (benign):4 | ||||
chr22:20917329-20917418 | Rare:26 | ||||
chr22:20982201-20982342 | Common:2; Rare:31; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr22:21002068-21002220 | Common:3; Rare:56 | ||||
chr22:21642068-21642366 | Common:2; Rare:91 | ||||
chr22:21938234-21938296 | Rare:28 | ||||
chr22:23750933-23751220 | Common:4; Rare:91 | ||||
chr22:23767940-23768037 | Rare:28 |