Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:34539599-34539909 | Common:1; Rare:88 | ||||
chr14:34629944-34630260 | Common:5; Rare:126 | ||||
chr14:34713503-34713761 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
chr14:34875264-34875546 | Common:1; Rare:103 | ||||
chr14:34982372-34982709 | Common:1; Rare:136 | ||||
chr14:35046130-35046580 | Common:1; Rare:153 | ||||
chr14:35121955-35122787 | Common:4; Rare:234 | ||||
chr14:35292232-35292486 | Common:4; Rare:95; Clinvar:1 | ||||
chr14:35402741-35403320 | Common:5; Rare:190; Clinvar:3; Clinvar (benign):4 | ||||
chr14:35403412-35403558 | Rare:33 | ||||
chr14:35404417-35404809 | Common:3; Rare:133; Clinvar:1; Clinvar (benign):5 | ||||
chr14:35826166-35826468 | Rare:78 | ||||
chr14:35826728-35826906 | Common:1; Rare:46 | ||||
chr14:36320557-36320764 | Common:4; Rare:76 | ||||
chr14:37197888-37198103 | Common:2; Rare:65 |