Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:109644654-109644907 | Common:1; Rare:79 | ||||
chr8:116755777-116755880 | Rare:57 | ||||
chr8:119832815-119832903 | Common:1; Rare:36 | ||||
chr8:119873564-119873849 | Common:3; Rare:84 | ||||
chr8:120445100-120445455 | Common:1; Rare:89 | ||||
chr8:120812001-120812118 | Common:1; Rare:22 | ||||
chr8:120812457-120812722 | Rare:50 | ||||
chr8:122781589-122781918 | Common:3; Rare:64 | ||||
chr8:123241335-123241455 | Common:1; Rare:48 | ||||
chr8:123416342-123416821 | Rare:126 | ||||
chr8:124372677-124372829 | Common:1; Rare:51 | ||||
chr8:124474521-124474778 | Common:1; Rare:95 | ||||
chr8:124474936-124475099 | Rare:48 | ||||
chr8:124539042-124539286 | Common:2; Rare:118; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr8:124728400-124728647 | Common:2; Rare:74 |