chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182492130324921304GA17GENIChomozygous110309502
182492276324922764TA30GENIChomozygous110309504
182492321924923220TG33GENICpossibly homozygous110309506
182492406924924070TG19GENIChomozygous110309508
182492500824925009CT20GENIChomozygous110309510
182492541424925415AG17GENIChomozygous110309512
182492572124925722AG25GENIChomozygous110309514
182492590324925904TG23GENIChomozygous110309516
182492607924926080CT22GENIChomozygous110309518
182492613324926134CT23GENIChomozygous110309520
182492616424926165TC25GENIChomozygous110309522
182492621124926212GA26GENICpossibly homozygous110309524
182492644624926447CT29GENICpossibly homozygous110309526
182492676724926768AG16GENIChomozygous110309528
182492740624927407GA36GENIChomozygous110309531
182492742724927428GA34GENIChomozygous110309533
182492749824927499AG26GENIChomozygous110309535
182492786524927866TC17GENIChomozygous110309538
182492813024928131AG30GENIChomozygous110309540