chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4133995812133995813TC14GENIChomozygous71151434
4133995934133995935GA37GENIChomozygous71151437
4133995982133995983CT35GENIChomozygous71151440
4133996073133996074TC38GENIChomozygous71151443
4133996166133996167AG42GENIChomozygous71151447
4133996323133996324CT36GENIChomozygous71151450
4133996637133996638TC20GENIChomozygous71151457
4133997177133997178AC25GENIChomozygous71151458
4133997365133997366CT32GENIChomozygous71151461
4133997750133997751TG16GENIChomozygous71151467
4133997922133997923CT15GENIChomozygous71151470
4133997988133997989GA23GENIChomozygous71622546
4133998138133998139CA19GENIChomozygous71151473
4133998188133998189AT14GENIChomozygous71151476
4133998461133998462TC20GENIChomozygous71151479
4133998609133998610TC29GENIChomozygous71151482
4133998646133998647CT30GENIChomozygous71151485
4133998648133998649GA30GENIChomozygous71151488
4133998681133998682GA35GENIChomozygous71151491
4133998692133998693TC40GENIChomozygous71151494
4133998742133998743GC30GENIChomozygous71151497
4133998818133998819AG25GENIChomozygous71151503
4133998917133998918AC19GENIChomozygous71151506
4133998994133998995TC19GENIChomozygous71151509
4133999336133999337CA16GENICheterozygous73915051
4133999338133999339CA14GENICpossibly homozygous73915054
4133999440133999441CT21GENIChomozygous71151512