Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:10354047-10354364 | Rare:109 | ||||
chr5:31532036-31532324 | Common:3; Rare:75 | ||||
chr5:33440642-33441083 | Common:6; Rare:122 | ||||
chr5:34915218-34915355 | Rare:38 | ||||
chr5:34915493-34915792 | Common:1; Rare:83 | ||||
chr5:36151897-36152195 | Rare:94 | ||||
chr5:36876650-36876906 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
chr5:38845739-38846067 | Common:2; Rare:88 | ||||
chr5:44808743-44808985 | Common:2; Rare:85 | ||||
chr5:50441257-50441427 | Common:2; Rare:53 | ||||
chr5:53109725-53109877 | Common:1; Rare:77; Clinvar:2 | ||||
chr5:55307639-55308010 | Common:4; Rare:122 | ||||
chr5:55534691-55534786 | Common:1; Rare:31 | ||||
chr5:60945004-60945335 | Common:6; Rare:129; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr5:61162395-61162613 | Common:1; Rare:65 |