chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91485397714853978CT57GENIChomozygous142131674
91485485014854851TC52GENIChomozygous142131675
91485485714854858TC56GENIChomozygous142131676
91485488214854883AG57GENIChomozygous138522594
91485500214855003TC62GENIChomozygous138522595
91485619514856196CG57GENIChomozygous142131677
91485720414857205CT27GENIChomozygous142131678
91485854814858549TG66GENIChomozygous142131679
91485973414859735AC47GENIChomozygous142131680
91486242214862423AC46GENIChomozygous142131681
91486287914862880TC56GENIChomozygous142131682
91486752714867528TG60GENIChomozygous142131683
91486792414867925GT58GENIChomozygous142131684
91486793914867940TC65GENIChomozygous142131685
91486812214868123GC30GENIChomozygous142131686
91486831714868318AG50GENIChomozygous142131687
91486832514868326AG51GENIChomozygous142131688
91486856314868564TA45GENIChomozygous142131689
91486908914869090CT37GENIChomozygous142131690
91486915414869155GT40GENICpossibly homozygous142131691
91486915514869156CT42GENICpossibly homozygous142131692
91485556914855569G58GENIChomozygous142109675
91486905414869055T40GENIChomozygous142109677