chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4133995812133995813TC31GENIChomozygous71151434
4133995934133995935GA34GENIChomozygous71151437
4133995982133995983CT36GENIChomozygous71151440
4133996073133996074TC44GENIChomozygous71151443
4133996166133996167AG36GENIChomozygous71151447
4133996323133996324CT33GENIChomozygous71151450
4133996637133996638TC38GENIChomozygous71151457
4133997177133997178AC22GENIChomozygous71151458
4133997365133997366CT29GENIChomozygous71151461
4133997750133997751TG26GENIChomozygous71151467
4133997922133997923CT24GENIChomozygous71151470
4133997988133997989GA27GENIChomozygous71622546
4133998138133998139CA29GENIChomozygous71151473
4133998188133998189AT27GENIChomozygous71151476
4133998461133998462TC30GENIChomozygous71151479
4133998609133998610TC36GENIChomozygous71151482
4133998646133998647CT38GENIChomozygous71151485
4133998648133998649GA39GENIChomozygous71151488
4133998681133998682GA38GENIChomozygous71151491
4133998692133998693TC37GENIChomozygous71151494
4133998742133998743GC32GENIChomozygous71151497
4133998818133998819AG44GENIChomozygous71151503
4133998917133998918AC22GENIChomozygous71151506
4133998994133998995TC27GENIChomozygous71151509
4133999440133999441CT26GENIChomozygous71151512
4133999338133999339CA18GENICpossibly homozygous73915054
4133999336133999337CA18GENICpossibly homozygous73915051