Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:35056210-35056287 | Common:2; Rare:13 | ||||
chr19:36142654-36142957 | Rare:79 | ||||
chr19:36797283-36797540 | Rare:54 | ||||
chr19:38375902-38376228 | Common:2; Rare:73 | ||||
chr19:38468963-38469513 | Common:3; Rare:148; Clinvar:20; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
chr19:39403704-39403924 | Rare:37 | ||||
chr19:41500604-41500776 | Common:1; Rare:30 | ||||
chr19:46860794-46861111 | Common:3; Rare:104 | ||||
chr19:48966279-48966724 | Rare:147; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr19:49073742-49074012 | Rare:56 | ||||
chr19:50435776-50436156 | Common:3; Rare:124 | ||||
chr19:50458739-50459305 | Common:3; Rare:221 | ||||
chr19:55147992-55148364 | Rare:82 | ||||
chr19:55546124-55546387 | Rare:48 | ||||
chr2:1154008-1154258 | Common:6; Rare:57 |