Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:9786042-9786219 | Rare:50 | ||||
chr19:9818778-9818866 | Rare:39 | ||||
chr19:9819047-9819184 | Common:1; Rare:36 | ||||
chr19:9827828-9827954 | Common:1; Rare:48 | ||||
chr19:10102941-10102994 | Rare:14 | ||||
chr19:10106182-10106415 | Common:1; Rare:83 | ||||
chr19:10271011-10271130 | Rare:32 | ||||
chr19:10333508-10333783 | Rare:84 | ||||
chr19:10380457-10380815 | Common:12; Rare:106; Clinvar:5 | ||||
chr19:10403390-10403732 | Rare:131 | ||||
chr19:10502706-10502919 | Rare:56 | ||||
chr19:10503304-10503419 | Rare:26 | ||||
chr19:10653810-10654132 | Common:1; Rare:123 | ||||
chr19:10928565-10928851 | Common:2; Rare:93 | ||||
chr19:10960680-10961161 | Common:4; Rare:178; Clinvar (benign):1 |