chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91485397714853978CT26GENIChomozygous142131674
91485485014854851TC21GENIChomozygous142131675
91485485714854858TC23GENIChomozygous142131676
91485488214854883AG23GENIChomozygous138522594
91485500214855003TC27GENIChomozygous138522595
91485619514856196CG31GENIChomozygous142131677
91485720414857205CT17GENIChomozygous142131678
91485854814858549TG21GENIChomozygous142131679
91485973414859735AC16GENIChomozygous142131680
91486242214862423AC23GENIChomozygous142131681
91486287914862880TC21GENIChomozygous142131682
91486752714867528TG25GENIChomozygous142131683
91486792414867925GT21GENIChomozygous142131684
91486793914867940TC21GENIChomozygous142131685
91486812214868123GC22GENIChomozygous142131686
91486831714868318AG25GENIChomozygous142131687
91486832514868326AG26GENIChomozygous142131688
91486856314868564TA18GENIChomozygous142131689
91486908914869090CT17GENIChomozygous142131690
91486915414869155GT18GENIChomozygous142131691
91486915514869156CT17GENIChomozygous142131692
91485556914855569G29GENIChomozygous142109675
91486905414869055T20GENIChomozygous142109677