Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:27793889-27794030 | Rare:32 | ||||
chr19:34860564-34860852 | Common:2; Rare:58 | ||||
chr19:35716943-35717154 | Common:3; Rare:41 | ||||
chr19:36142652-36142953 | Rare:81 | ||||
chr19:36160655-36160977 | Rare:93 | ||||
chr19:36331639-36331948 | Common:2; Rare:81 | ||||
chr19:36797283-36797554 | Common:1; Rare:59 | ||||
chr19:38666109-38666414 | Common:1; Rare:71 | ||||
chr19:40980912-40981115 | Rare:31 | ||||
chr19:44849210-44849489 | Common:1; Rare:45 | ||||
chr19:46133322-46133608 | Rare:49 | ||||
chr19:46860835-46861115 | Common:3; Rare:90 | ||||
chr19:48398803-48399093 | Rare:59 | ||||
chr19:48966277-48966672 | Rare:128; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr19:49491486-49491794 | Common:1; Rare:101 |