Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:67481084-67481369 | Common:1; Rare:110 | ||||
chr16:67528636-67528883 | Rare:62 | ||||
chr16:67806529-67806858 | Rare:66 | ||||
chr16:68023223-68023335 | Common:1; Rare:27 | ||||
chr16:68245186-68245402 | Common:1; Rare:67 | ||||
chr16:68310930-68311084 | Common:1; Rare:77 | ||||
chr16:69132111-69132343 | Rare:45 | ||||
chr16:69132521-69132680 | Rare:62 | ||||
chr16:69339545-69339841 | Common:1; Rare:128; Clinvar:1; Clinvar (benign):1 | ||||
chr16:69424462-69424681 | Common:1; Rare:61 | ||||
chr16:69726444-69726863 | Common:3; Rare:111 | ||||
chr16:70289434-70289740 | Rare:111; Clinvar:1 | ||||
chr16:70346750-70346986 | Common:2; Rare:118 | ||||
chr16:70523517-70523864 | Common:3; Rare:116; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr16:71289202-71289453 | Common:2; Rare:66 |