Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:70205659-70205750 | Common:2; Rare:43; Clinvar (benign):2 | ||||
chr18:74148276-74148573 | Common:2; Rare:113 | ||||
chr18:74597613-74597889 | Common:2; Rare:73 | ||||
chr18:79988375-79988645 | Common:3; Rare:102; Clinvar (pathogenic):2 | ||||
chr19:572237-572636 | Common:3; Rare:199 | ||||
chr19:633505-633724 | Common:8; Rare:109 | ||||
chr19:1103755-1104115 | Common:7; Rare:152 | ||||
chr19:1905184-1905427 | Common:4; Rare:100 | ||||
chr19:2328559-2328701 | Common:1; Rare:68 | ||||
chr19:2783250-2783456 | Rare:74 | ||||
chr19:2944922-2945181 | Common:5; Rare:88 | ||||
chr19:3366439-3366630 | Common:4; Rare:52 | ||||
chr19:3979139-3979336 | Common:2; Rare:69 | ||||
chr19:3982805-3983210 | Common:5; Rare:142; Clinvar:1; Clinvar (benign):3 | ||||
chr19:4723755-4724067 | Common:6; Rare:119 |