Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:47780424-47780747 | Common:2; Rare:82 | ||||
chr19:48170300-48170704 | Common:2; Rare:105 | ||||
chr19:48255896-48255971 | Common:4; Rare:13 | ||||
chr19:48390431-48390757 | Common:4; Rare:88 | ||||
chr19:48445900-48446177 | Common:1; Rare:113 | ||||
chr19:48619139-48619435 | Rare:96 | ||||
chr19:48918723-48919122 | Common:3; Rare:129 | ||||
chr19:48954596-48954925 | Common:1; Rare:116 | ||||
chr19:48965357-48965609 | Rare:80; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr19:48993237-48993912 | Common:8; Rare:236; Clinvar:3; Clinvar (benign):2 | ||||
chr19:49085126-49085492 | Common:3; Rare:146 | ||||
chr19:49157578-49157859 | Common:3; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
chr19:49453069-49453311 | Common:1; Rare:79 | ||||
chr19:49453480-49453588 | Rare:30 | ||||
chr19:49496224-49496496 | Common:1; Rare:104 |