Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:46267836-46268029 | Common:1; Rare:56 | ||||
chr22:46296636-46296964 | Common:2; Rare:109 | ||||
chr22:46738212-46738439 | Common:6; Rare:55 | ||||
chr22:46762526-46762712 | Common:3; Rare:66 | ||||
chr22:49918302-49918698 | Common:4; Rare:138; Clinvar (benign):3 | ||||
chr22:50278625-50278964 | Common:1; Rare:92 | ||||
chr22:50307566-50307671 | Rare:37 | ||||
chr22:50343192-50343402 | Common:2; Rare:87 | ||||
chr22:50481468-50481546 | Rare:22 | ||||
chr22:50526622-50526844 | Common:1; Rare:94; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
chr22:50582779-50583124 | Common:7; Rare:110; Clinvar:2; Clinvar (benign):3 | ||||
chr22:50628107-50628286 | Common:9; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
chr22:50783598-50783822 | Common:2; Rare:73 | ||||
chr3:3126810-3126981 | Common:4; Rare:72; Clinvar (benign):1 | ||||
chr3:4303253-4303427 | Common:1; Rare:67 |