Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:76306547-76306742 | Rare:56 | ||||
chr4:76738610-76738842 | Common:1; Rare:68 | ||||
chr4:76948762-76949068 | Common:2; Rare:67 | ||||
chr4:77032409-77032552 | Common:1; Rare:28 | ||||
chr4:77032555-77032882 | Rare:51 | ||||
chr4:77033486-77033668 | Rare:29 | ||||
chr4:84499339-84499593 | Rare:79 | ||||
chr4:88019551-88019674 | Rare:23 | ||||
chr4:88046711-88047100 | Rare:99; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr4:113980376-113980623 | Rare:42 | ||||
chr4:118279673-118279701 | Common:1; Rare:7 | ||||
chr4:118279746-118279788 | Common:1; Rare:7 | ||||
chr4:118279806-118280046 | Common:2; Rare:60 | ||||
chr4:118307986-118308129 | Rare:26 | ||||
chr4:118352213-118352469 | Rare:91; Clinvar:4 |