Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:7294238-7294522 | Common:6; Rare:69 | ||||
chr19:7395041-7395218 | Common:4; Rare:56 | ||||
chr19:7489000-7489210 | Common:2; Rare:86 | ||||
chr19:7506673-7506921 | Common:2; Rare:29 | ||||
chr19:7515895-7516249 | Rare:81 | ||||
chr19:7533878-7534219 | Common:3; Rare:85; Clinvar (benign):1 | ||||
chr19:7535569-7535791 | Common:3; Rare:81 | ||||
chr19:7541238-7541372 | Rare:41; Clinvar:1 | ||||
chr19:7614207-7614308 | Rare:11 | ||||
chr19:7629495-7629879 | Common:7; Rare:142; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7636953-7637185 | Common:2; Rare:68; Clinvar (benign):1 | ||||
chr19:7903512-7903962 | Common:2; Rare:146 | ||||
chr19:7920216-7920411 | Rare:84 | ||||
chr19:7932748-7932890 | Common:3; Rare:60; Clinvar (benign):1 | ||||
chr19:7943627-7943995 | Rare:103 |