Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:17159190-17159359 | Common:5; Rare:75 | ||||
chr22:17628680-17628895 | Common:1; Rare:81 | ||||
chr22:18077802-18078035 | Common:5; Rare:76; Clinvar:3; Clinvar (benign):2 | ||||
chr22:18110658-18110835 | Rare:46 | ||||
chr22:19432345-19432595 | Common:2; Rare:105 | ||||
chr22:19447677-19447852 | Common:2; Rare:75 | ||||
chr22:19479107-19479466 | Common:4; Rare:132 | ||||
chr22:19479687-19479987 | Common:4; Rare:84 | ||||
chr22:19854787-19855023 | Rare:89 | ||||
chr22:19881858-19882166 | Common:3; Rare:51 | ||||
chr22:19941709-19942124 | Common:2; Rare:121; Clinvar:6; Clinvar (benign):4 | ||||
chr22:20020873-20021151 | Common:1; Rare:94 | ||||
chr22:20117181-20117653 | Common:4; Rare:153 | ||||
chr22:20319998-20320141 | Common:1; Rare:50 | ||||
chr22:20495781-20495985 | Common:2; Rare:78 |