chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4133995812133995813TC5GENIChomozygous71151434
4133995934133995935GA9GENIChomozygous71151437
4133995982133995983CT5GENIChomozygous71151440
4133996073133996074TC14GENIChomozygous71151443
4133996166133996167AG8GENIChomozygous71151447
4133996323133996324CT6GENIChomozygous71151450
4133996637133996638TC11GENIChomozygous71151457
4133997177133997178AC17GENIChomozygous71151458
4133997365133997366CT2GENIChomozygous71151461
4133997750133997751TG9GENIChomozygous71151467
4133997922133997923CT9GENIChomozygous71151470
4133997988133997989GA5GENIChomozygous71622546
4133998138133998139CA19GENIChomozygous71151473
4133998188133998189AT8GENIChomozygous71151476
4133998461133998462TC7GENIChomozygous71151479
4133998609133998610TC14GENIChomozygous71151482
4133998646133998647CT11GENIChomozygous71151485
4133998648133998649GA11GENIChomozygous71151488
4133998681133998682GA11GENIChomozygous71151491
4133998692133998693TC10GENIChomozygous71151494
4133998742133998743GC5GENIChomozygous71151497
4133998818133998819AG6GENIChomozygous71151503
4133998917133998918AC11GENIChomozygous71151506
4133998994133998995TC6GENIChomozygous71151509
4133999440133999441CT14GENIChomozygous71151512
4133999338133999339CA5GENICheterozygous73915054
4133999336133999337CA3GENICheterozygous73915051