Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49640032-49640336 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
chr19:49851096-49851182 | Common:1; Rare:30 | ||||
chr19:49877293-49877720 | Common:1; Rare:108 | ||||
chr19:49877836-49878221 | Common:5; Rare:127 | ||||
chr19:49929119-49929212 | Common:3; Rare:29 | ||||
chr19:49929405-49929586 | Common:4; Rare:65 | ||||
chr19:50476405-50476543 | Rare:66 | ||||
chr19:51887965-51888047 | Rare:32 | ||||
chr19:52397661-52397882 | Common:3; Rare:61 | ||||
chr19:54115265-54115423 | Common:1; Rare:37; Clinvar (benign):1 | ||||
chr19:54115635-54115797 | Common:1; Rare:37; Clinvar:4 | ||||
chr19:54449039-54449225 | Common:2; Rare:50 | ||||
chr19:55385737-55385976 | Common:6; Rare:81 | ||||
chr19:55485107-55485242 | Common:1; Rare:50 | ||||
chr19:55643349-55643651 | Common:4; Rare:88 |