Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:46635461-46635693 | Common:6; Rare:77 | ||||
chr22:17628712-17628860 | Common:1; Rare:47 | ||||
chr22:17638677-17638817 | Rare:49 | ||||
chr22:18077820-18078014 | Common:3; Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
chr22:19432284-19432604 | Common:4; Rare:138 | ||||
chr22:19447676-19447866 | Common:2; Rare:78 | ||||
chr22:19479675-19479956 | Common:4; Rare:74 | ||||
chr22:19854787-19854972 | Rare:63 | ||||
chr22:19941746-19941886 | Rare:56; Clinvar:4 | ||||
chr22:20117193-20117655 | Common:4; Rare:147 | ||||
chr22:20319992-20320158 | Common:2; Rare:55 | ||||
chr22:20858705-20859102 | Common:6; Rare:200; Clinvar:3; Clinvar (benign):3 | ||||
chr22:20917132-20917418 | Rare:97 | ||||
chr22:20982196-20982358 | Common:2; Rare:37; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr22:21002106-21002205 | Common:3; Rare:31 |