Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:27793667-27794066 | Common:1; Rare:101 | ||||
chr19:35003379-35003631 | Rare:61 | ||||
chr19:36331681-36331934 | Common:2; Rare:64 | ||||
chr19:36797273-36797542 | Rare:58 | ||||
chr19:41531561-41531707 | Common:1; Rare:35 | ||||
chr19:48966401-48966624 | Rare:67 | ||||
chr19:50051029-50051147 | Rare:18 | ||||
chr2:20448385-20448711 | Common:1; Rare:81 | ||||
chr2:54673629-54673885 | Common:3; Rare:64 | ||||
chr2:55923033-55923169 | Rare:29 | ||||
chr2:74377442-74377689 | Common:1; Rare:63 | ||||
chr2:85667096-85667240 | Common:1; Rare:44; Clinvar (benign):1 | ||||
chr2:88016540-88016817 | Common:10; Rare:118 | ||||
chr2:88857445-88857619 | Rare:58 | ||||
chr2:89040716-89040828 | Common:2; Rare:19 |