chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4133995812133995813TC54GENICpossibly homozygous71151434
4133995934133995935GA35GENIChomozygous71151437
4133995982133995983CT33GENIChomozygous71151440
4133996073133996074TC39GENICpossibly homozygous71151443
4133996166133996167AG27GENIChomozygous71151447
4133996323133996324CT32GENICpossibly homozygous71151450
4133996637133996638TC48GENIChomozygous71151457
4133997177133997178AC24GENICpossibly homozygous71151458
4133997365133997366CT20GENIChomozygous71151461
4133997750133997751TG37GENIChomozygous71151467
4133997922133997923CT22GENIChomozygous71151470
4133997988133997989GA27GENIChomozygous71622546
4133998138133998139CA21GENIChomozygous71151473
4133998188133998189AT39GENIChomozygous71151476
4133998461133998462TC24GENIChomozygous71151479
4133998609133998610TC40GENIChomozygous71151482
4133998646133998647CT25GENIChomozygous71151485
4133998648133998649GA28GENIChomozygous71151488
4133998681133998682GA49GENIChomozygous71151491
4133998692133998693TC30GENIChomozygous71151494
4133998742133998743GC30GENIChomozygous71151497
4133998818133998819AG32GENIChomozygous71151503
4133998917133998918AC30GENIChomozygous71151506
4133998994133998995TC33GENIChomozygous71151509
4133999440133999441CT24GENIChomozygous71151512