Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:41216659-41216830 | Common:2; Rare:27 | ||||
chr4:41360715-41360837 | Common:1; Rare:37 | ||||
chr4:41990379-41990590 | Common:1; Rare:77 | ||||
chr4:42397910-42398025 | Common:1; Rare:22 | ||||
chr4:44678352-44678714 | Common:1; Rare:133 | ||||
chr4:44726481-44726649 | Common:2; Rare:59 | ||||
chr4:47485142-47485449 | Common:2; Rare:89 | ||||
chr4:48269807-48269981 | Common:1; Rare:35 | ||||
chr4:48780197-48780572 | Common:3; Rare:114 | ||||
chr4:51842810-51843239 | Common:1; Rare:131 | ||||
chr4:51843382-51843695 | Rare:87 | ||||
chr4:52038228-52038324 | Rare:44; Clinvar:10; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
chr4:52659188-52659442 | Common:1; Rare:86 | ||||
chr4:53365980-53366204 | Rare:52 | ||||
chr4:55125464-55125694 | Common:3; Rare:53 |