Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45406363-45406687 | Common:2; Rare:81 | ||||
chr19:45423450-45423708 | Common:2; Rare:56; Clinvar (benign):1 | ||||
chr19:45496949-45497272 | Common:2; Rare:97 | ||||
chr19:45507227-45507510 | Common:1; Rare:72 | ||||
chr19:45692372-45692678 | Common:1; Rare:65 | ||||
chr19:46346951-46347128 | Common:3; Rare:51 | ||||
chr19:46601004-46601402 | Common:4; Rare:129 | ||||
chr19:46717075-46717206 | Common:1; Rare:39 | ||||
chr19:46745960-46746061 | Common:3; Rare:26 | ||||
chr19:47256472-47256583 | Rare:42 | ||||
chr19:47484261-47484318 | Rare:14 | ||||
chr19:48170270-48170699 | Common:2; Rare:116 | ||||
chr19:48325326-48325609 | Common:2; Rare:63 | ||||
chr19:48445854-48446014 | Rare:54 | ||||
chr19:48619139-48619537 | Common:1; Rare:134 |