Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:39498686-39498968 | Common:2; Rare:72; Clinvar:1 | ||||
chr19:39515286-39515441 | Rare:57 | ||||
chr19:39540108-39540366 | Common:2; Rare:62 | ||||
chr19:39833491-39833896 | Common:2; Rare:131 | ||||
chr19:39834124-39834556 | Common:3; Rare:122 | ||||
chr19:39846298-39846478 | Common:1; Rare:85 | ||||
chr19:39970957-39971223 | Common:3; Rare:73 | ||||
chr19:39996947-39997118 | Common:5; Rare:58 | ||||
chr19:40056150-40056375 | Rare:37 | ||||
chr19:40090747-40091016 | Common:1; Rare:66 | ||||
chr19:40191350-40191482 | Common:2; Rare:38 | ||||
chr19:40285243-40285462 | Common:1; Rare:78 | ||||
chr19:40348324-40348758 | Common:4; Rare:139 | ||||
chr19:40377873-40378145 | Common:2; Rare:93; Clinvar (benign):1 | ||||
chr19:40413336-40413543 | Rare:60 |