Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:54902104-54902248 | Common:1; Rare:49 | ||||
chr14:54902824-54902958 | Rare:37; Clinvar (benign):1 | ||||
chr14:55027080-55027326 | Common:2; Rare:66 | ||||
chr14:57268649-57269072 | Common:2; Rare:139 | ||||
chr14:58244661-58244923 | Rare:85 | ||||
chr14:58298106-58298630 | Rare:138 | ||||
chr14:58427116-58427394 | Rare:64 | ||||
chr14:58427529-58427733 | Rare:66 | ||||
chr14:59188437-59188708 | Rare:62 | ||||
chr14:59484365-59484558 | Common:2; Rare:62 | ||||
chr14:60981047-60981283 | Rare:85 | ||||
chr14:61476903-61477134 | Common:3; Rare:44 | ||||
chr14:61695234-61695588 | Common:3; Rare:105 | ||||
chr14:61740509-61740751 | Rare:66 | ||||
chr14:63641838-63642188 | Common:6; Rare:114 |