Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:37594739-37594848 | Rare:35 | ||||
chr19:37779594-37779662 | Rare:11 | ||||
chr19:37907062-37907300 | Rare:53 | ||||
chr19:37932318-37932641 | Common:2; Rare:64 | ||||
chr19:38264325-38264705 | Common:5; Rare:99 | ||||
chr19:38315804-38316244 | Common:1; Rare:131 | ||||
chr19:38618947-38619252 | Common:3; Rare:90 | ||||
chr19:38647372-38647854 | Common:3; Rare:159 | ||||
chr19:38831755-38832045 | Common:4; Rare:90; Clinvar (benign):1 | ||||
chr19:38899572-38900033 | Rare:137 | ||||
chr19:38930722-38931013 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39390953-39391425 | Common:1; Rare:176 | ||||
chr19:39406706-39406868 | Rare:63 | ||||
chr19:39480591-39480925 | Common:3; Rare:160; Clinvar (pathogenic):1 | ||||
chr19:39846308-39846483 | Common:1; Rare:82 |