chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X140876237140876238GA9GENIChomozygous108455983
X140876558140876559AG8GENIChomozygous108347404
X140876903140876904TC10GENIChomozygous108455985
X140877384140877385CG17GENIChomozygous108347406
X140878408140878409AG9GENIChomozygous108347408
X140878413140878414CG9GENIChomozygous108347410
X140881236140881237CT11GENIChomozygous108347412
X140884219140884220GA16GENIChomozygous108347414
X140886025140886026GT16GENIChomozygous108347420
X140886446140886447TC11GENIChomozygous108347424
X140886772140886773AG9GENIChomozygous108347426
X140887772140887773CG14GENIChomozygous108347428
X140887956140887957CT10GENIChomozygous108347430
X140885858140885859GA9GENIChomozygous108553359
X140883107140883108A10GENIChomozygous129796528
X140884598140884599T9GENIChomozygous129796529
X140886836140886839TTC4GENIChomozygous129796531
X140883256140883257A20GENICpossibly homozygous131971016