Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58059184-58059287 | Rare:55 | ||||
chr19:58098200-58098474 | Common:8; Rare:102 | ||||
chr19:58155033-58155296 | Common:3; Rare:68 | ||||
chr19:58183274-58183442 | Rare:59 | ||||
chr19:58228826-58228946 | Common:1; Rare:48 | ||||
chr19:58278600-58278998 | Common:4; Rare:122 | ||||
chr19:58326873-58327064 | Common:1; Rare:45 | ||||
chr19:58327208-58327356 | Rare:36 | ||||
chr19:58347552-58347780 | Common:8; Rare:102 | ||||
chr19:58362502-58362614 | Rare:35 | ||||
chr19:58386734-58386807 | Common:1; Rare:20 | ||||
chr19:58408449-58408692 | Common:3; Rare:75 | ||||
chr19:58440134-58440448 | Common:6; Rare:82 | ||||
chr19:58475993-58476169 | Common:1; Rare:70 | ||||
chr19:58499211-58499632 | Common:2; Rare:148; Clinvar:6; Clinvar (benign):1 |