Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:62186956-62187328 | Common:5; Rare:103 | ||||
chr18:63367133-63367351 | Common:1; Rare:82 | ||||
chr18:63422370-63422660 | Common:1; Rare:78 | ||||
chr18:68714987-68715260 | Common:5; Rare:123 | ||||
chr18:70205659-70205871 | Common:3; Rare:84; Clinvar (benign):2 | ||||
chr18:74148353-74148573 | Common:1; Rare:71 | ||||
chr18:74291865-74292284 | Common:4; Rare:126 | ||||
chr18:74597601-74597907 | Common:2; Rare:79 | ||||
chr18:76822226-76822585 | Common:11; Rare:98 | ||||
chr18:79988262-79988651 | Common:3; Rare:125; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr19:344784-344925 | Common:3; Rare:45 | ||||
chr19:572237-572644 | Common:3; Rare:205 | ||||
chr19:633520-633730 | Common:8; Rare:98 | ||||
chr19:663143-663423 | Common:2; Rare:111 | ||||
chr19:893167-893484 | Common:3; Rare:132 |