Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:39114264-39114333 | Common:2; Rare:29 | ||||
chr14:39174904-39175285 | Common:5; Rare:133 | ||||
chr14:39267037-39267414 | Common:2; Rare:126 | ||||
chr14:39432453-39432650 | Common:6; Rare:69 | ||||
chr14:41606842-41607118 | Common:4; Rare:83 | ||||
chr14:41607534-41607612 | Common:2; Rare:15 | ||||
chr14:41608179-41608359 | Rare:42 | ||||
chr14:44961892-44962255 | Common:3; Rare:105 | ||||
chr14:45135723-45135979 | Common:1; Rare:48 | ||||
chr14:45253057-45253282 | Rare:62 | ||||
chr14:49586314-49586776 | Common:1; Rare:243; Clinvar (benign):1 | ||||
chr14:49598656-49599014 | Common:2; Rare:138 | ||||
chr14:49620574-49620830 | Common:2; Rare:105; Clinvar:3 | ||||
chr14:49688201-49688272 | Rare:26 | ||||
chr14:49693054-49693185 | Common:1; Rare:50 |