Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:25160415-25160704 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
chr4:25233853-25234047 | Rare:86 | ||||
chr4:26320586-26320850 | Common:1; Rare:103 | ||||
chr4:37826574-37826729 | Common:1; Rare:57 | ||||
chr4:39458834-39459093 | Common:3; Rare:139; Clinvar (benign):4 | ||||
chr4:39638850-39639140 | Common:1; Rare:109 | ||||
chr4:41256738-41257005 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr4:41990420-41990539 | Common:1; Rare:44 | ||||
chr4:44678395-44678487 | Rare:32 | ||||
chr4:48016643-48016794 | Common:1; Rare:45 | ||||
chr4:56435600-56435797 | Common:1; Rare:61 | ||||
chr4:56467542-56467641 | Rare:38 | ||||
chr4:56977518-56977739 | Common:2; Rare:81 | ||||
chr4:57110061-57110177 | Rare:43 | ||||
chr4:67701118-67701379 | Common:4; Rare:120 |