Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:18651543-18651725 | Common:1; Rare:75 | ||||
chr10:18659099-18659419 | Common:3; Rare:94 | ||||
chr10:22316187-22316459 | Common:2; Rare:117 | ||||
chr10:24208857-24209184 | Rare:93 | ||||
chr10:27154310-27154486 | Rare:48 | ||||
chr10:27155155-27155391 | Common:4; Rare:81; Clinvar:5; Clinvar (benign):4 | ||||
chr10:27240485-27240638 | Common:2; Rare:51 | ||||
chr10:27240767-27240877 | Rare:28 | ||||
chr10:27242058-27242218 | Common:1; Rare:68 | ||||
chr10:28532496-28532862 | Common:5; Rare:147 | ||||
chr10:29634929-29635061 | Rare:26 | ||||
chr10:30434607-30434693 | Common:1; Rare:27 | ||||
chr10:31031846-31032052 | Common:2; Rare:83 | ||||
chr10:31318439-31318805 | Common:2; Rare:92 | ||||
chr10:31318812-31318921 | Rare:32 |