Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:35046119-35046462 | Common:2; Rare:113 | ||||
chr14:35121955-35122625 | Common:3; Rare:191 | ||||
chr14:35292179-35292473 | Common:5; Rare:106; Clinvar:1 | ||||
chr14:39170353-39170707 | Common:3; Rare:105 | ||||
chr14:39175002-39175272 | Common:3; Rare:93 | ||||
chr14:49586341-49586692 | Common:1; Rare:183 | ||||
chr14:49598901-49598996 | Rare:29 | ||||
chr14:49620570-49620797 | Common:2; Rare:89 | ||||
chr14:49892913-49893100 | Rare:73 | ||||
chr14:50116557-50116695 | Rare:63 | ||||
chr14:50312201-50312374 | Rare:66 | ||||
chr14:50944399-50944550 | Common:3; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
chr14:52707045-52707240 | Common:1; Rare:87 | ||||
chr14:52729841-52730231 | Common:2; Rare:124 | ||||
chr14:53956736-53957006 | Rare:62; Clinvar:1 |