Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:46601200-46601364 | Common:3; Rare:46 | ||||
chr19:48619139-48619280 | Rare:56 | ||||
chr19:50025384-50025725 | Common:5; Rare:101 | ||||
chr19:52397750-52397879 | Common:2; Rare:38 | ||||
chr19:54115649-54115787 | Common:1; Rare:27; Clinvar:4 | ||||
chr19:55149159-55149341 | Common:2; Rare:62; Clinvar (benign):1 | ||||
chr19:56368283-56368342 | Common:1; Rare:18 | ||||
chr19:56478060-56478187 | Rare:49 | ||||
chr19:57279879-57279984 | Rare:30 | ||||
chr19:58098208-58098509 | Common:9; Rare:107 | ||||
chr19:58347605-58347762 | Common:7; Rare:74 | ||||
chr2:3558269-3558663 | Common:6; Rare:141 | ||||
chr2:9423451-9423658 | Rare:68 | ||||
chr2:9555765-9556091 | Common:2; Rare:106 | ||||
chr2:17753715-17753858 | Common:1; Rare:54 |