Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:18153030-18153287 | Common:1; Rare:87 | ||||
chr19:18280084-18280500 | Common:4; Rare:156 | ||||
chr19:18280566-18281074 | Rare:174 | ||||
chr19:18281619-18281834 | Common:2; Rare:76 | ||||
chr19:18919335-18919783 | Common:3; Rare:172 | ||||
chr19:19033456-19033610 | Common:2; Rare:59 | ||||
chr19:19192095-19192264 | Common:1; Rare:54 | ||||
chr19:19192628-19193003 | Common:3; Rare:86; Clinvar (benign):1 | ||||
chr19:19320480-19320872 | Common:4; Rare:144 | ||||
chr19:19516120-19516258 | Rare:82; Clinvar (pathogenic):1 | ||||
chr19:19821708-19821909 | Common:1; Rare:65 | ||||
chr19:19865686-19865926 | Common:2; Rare:65 | ||||
chr19:19900795-19900959 | Rare:38 | ||||
chr19:21082061-21082248 | Rare:42 | ||||
chr19:21141731-21142085 | Common:1; Rare:90 |