Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:66934163-66934494 | Common:2; Rare:133 | ||||
chr16:67227014-67227156 | Rare:54 | ||||
chr16:67481084-67481368 | Common:1; Rare:110 | ||||
chr16:67528706-67528861 | Rare:43 | ||||
chr16:67660227-67660358 | Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
chr16:67806517-67806859 | Rare:73 | ||||
chr16:68023225-68023302 | Common:1; Rare:17 | ||||
chr16:68310927-68311084 | Common:1; Rare:78 | ||||
chr16:69132532-69132676 | Rare:58 | ||||
chr16:69339545-69339826 | Common:1; Rare:118; Clinvar:1; Clinvar (benign):1 | ||||
chr16:69726453-69726819 | Common:3; Rare:95 | ||||
chr16:70523524-70523890 | Common:3; Rare:120; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr16:72093598-72093851 | Rare:64 | ||||
chr16:75647638-75647863 | Common:4; Rare:109; Clinvar:3 | ||||
chr16:75648067-75648259 | Rare:80 |