Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:19941746-19941881 | Rare:53; Clinvar:4 | ||||
chr22:20020927-20021128 | Common:1; Rare:63 | ||||
chr22:20117163-20117646 | Common:3; Rare:157 | ||||
chr22:20319998-20320179 | Common:1; Rare:62 | ||||
chr22:20495787-20495973 | Common:2; Rare:68 | ||||
chr22:20858741-20859105 | Common:6; Rare:184; Clinvar:3; Clinvar (benign):4 | ||||
chr22:20982196-20982353 | Common:2; Rare:36; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr22:21002098-21002195 | Common:3; Rare:31 | ||||
chr22:21629997-21630043 | Common:1; Rare:23 | ||||
chr22:21642068-21642341 | Common:2; Rare:80 | ||||
chr22:23894577-23894789 | Common:3; Rare:79 | ||||
chr22:24011261-24011335 | Rare:19 | ||||
chr22:24270700-24270962 | Common:3; Rare:94 | ||||
chr22:24555077-24555428 | Common:3; Rare:124 | ||||
chr22:24555864-24556061 | Rare:58 |