Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24078240-24078428 | Common:1; Rare:43 | ||||
chr14:24173314-24173537 | Rare:67 | ||||
chr14:26598313-26598643 | Common:1; Rare:61 | ||||
chr14:27528468-27528653 | Common:1; Rare:31 | ||||
chr14:28410367-28410671 | Common:1; Rare:51 | ||||
chr14:28764336-28764714 | Common:1; Rare:88 | ||||
chr14:28766009-28766230 | Rare:54 | ||||
chr14:28766287-28766365 | Common:1; Rare:17 | ||||
chr14:28766412-28766768 | Common:2; Rare:129 | ||||
chr14:28767453-28767953 | Common:4; Rare:142; Clinvar:14; Clinvar (benign):38; Clinvar (pathogenic):6 | ||||
chr14:28767955-28768094 | Rare:16; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:28768189-28768641 | Rare:104; Clinvar:3; Clinvar (benign):15; Clinvar (pathogenic):3 | ||||
chr14:28768709-28768885 | Common:2; Rare:35; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:28772661-28772854 | Rare:43 | ||||
chr14:28773004-28773226 | Common:2; Rare:39 |