Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49877299-49877717 | Common:1; Rare:106 | ||||
chr19:49929430-49929560 | Common:4; Rare:47 | ||||
chr19:50476392-50476539 | Rare:69 | ||||
chr19:50723178-50723414 | Common:2; Rare:55 | ||||
chr19:51366333-51366562 | Common:5; Rare:62; Clinvar (benign):2 | ||||
chr19:52008173-52008290 | Rare:35 | ||||
chr19:52028335-52028475 | Common:3; Rare:29 | ||||
chr19:52297056-52297198 | Common:16; Rare:36 | ||||
chr19:52397750-52397898 | Common:4; Rare:49 | ||||
chr19:53132869-53132927 | Common:2; Rare:18 | ||||
chr19:53254808-53255019 | Common:1; Rare:71 | ||||
chr19:54102678-54102887 | Common:3; Rare:56 | ||||
chr19:54115289-54115425 | Common:1; Rare:30; Clinvar (benign):1 | ||||
chr19:54115628-54115792 | Common:1; Rare:40; Clinvar:4 | ||||
chr19:54200728-54200901 | Common:4; Rare:70 |