Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:19033805-19033925 | Common:1; Rare:34 | ||||
chr19:19192104-19192268 | Common:1; Rare:52 | ||||
chr19:19192562-19192968 | Common:2; Rare:108 | ||||
chr19:19320476-19320884 | Common:4; Rare:160 | ||||
chr19:19516167-19516302 | Rare:79; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr19:19821645-19821878 | Common:1; Rare:78 | ||||
chr19:19900763-19900953 | Rare:54 | ||||
chr19:20565746-20565959 | Rare:58 | ||||
chr19:21505463-21505637 | Rare:40 | ||||
chr19:23395383-23395682 | Common:2; Rare:93 | ||||
chr19:29213114-29213233 | Common:1; Rare:43 | ||||
chr19:29665252-29665523 | Common:4; Rare:99 | ||||
chr19:29715041-29715332 | Common:1; Rare:112 | ||||
chr19:31349212-31349522 | Common:4; Rare:104 | ||||
chr19:32405551-32405806 | Rare:110 |