chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182491948224919483TG14GENICheterozygous119485418
182492058224920591CCACCCCAG3GENIChomozygous129524586
182492061624920617AT6GENIChomozygous110812143
182492104624921047GA10GENIChomozygous110309500
182492130324921304GA18GENIChomozygous110309502
182492276324922764TA24GENIChomozygous110309504
182492313424923134GTGTGTAT15GENIChomozygous129524587
182492321924923220TG16GENICpossibly homozygous110309506
182492361524923616AG19GENIChomozygous110647580
182492406924924070TG19GENIChomozygous110309508
182492500824925009CT17GENIChomozygous110309510
182492541424925415AG18GENIChomozygous110309512
182492572124925722AG17GENIChomozygous110309514
182492590324925904TG18GENIChomozygous110309516
182492607924926080CT16GENIChomozygous110309518
182492613324926134CT19GENIChomozygous110309520
182492616424926165TC19GENIChomozygous110309522
182492621124926212GA20GENIChomozygous110309524
182492644624926447CT16GENIChomozygous110309526
182492676724926768AG16GENIChomozygous110309528
182492740624927407GA26GENIChomozygous110309531
182492742724927428GA24GENIChomozygous110309533
182492748324927484A20GENIChomozygous129524588
182492749824927499AG20GENIChomozygous110309535
182492786524927866TC21GENIChomozygous110309538
182492813024928131AG15GENIChomozygous110309540