Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:52787823-52787951 | Common:1; Rare:20 | ||||
chr5:52989216-52989365 | Common:4; Rare:41; Clinvar (benign):1 | ||||
chr5:53109725-53109909 | Common:1; Rare:92; Clinvar:2 | ||||
chr5:55160080-55160200 | Rare:29 | ||||
chr5:55307625-55308016 | Common:4; Rare:132 | ||||
chr5:55534949-55535162 | Common:1; Rare:71 | ||||
chr5:55994888-55995196 | Rare:109 | ||||
chr5:56909466-56909637 | Common:2; Rare:49 | ||||
chr5:57173611-57174118 | Common:2; Rare:172 | ||||
chr5:58460046-58460184 | Common:3; Rare:59 | ||||
chr5:60700074-60700237 | Common:1; Rare:65 | ||||
chr5:60945026-60945258 | Common:5; Rare:87; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr5:61162359-61162613 | Common:1; Rare:68 | ||||
chr5:62403803-62404052 | Common:3; Rare:91 | ||||
chr5:62412557-62412781 | Rare:72 |