chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4133995812133995813TC28GENIChomozygous71151434
4133995934133995935GA14GENIChomozygous71151437
4133995982133995983CT15GENIChomozygous71151440
4133996073133996074TC29GENIChomozygous71151443
4133996166133996167AG57GENIChomozygous71151447
4133996323133996324CT51GENIChomozygous71151450
4133996637133996638TC32GENIChomozygous71151457
4133997177133997178AC19GENIChomozygous71151458
4133997365133997366CT58GENIChomozygous71151461
4133997750133997751TG11GENIChomozygous71151467
4133997782133997783TA10GENICheterozygous71622544
4133997922133997923CT29GENIChomozygous71151470
4133997988133997989GA25GENIChomozygous71622546
4133998138133998139CA13GENIChomozygous71151473
4133998188133998189AT12GENIChomozygous71151476
4133998461133998462TC12GENIChomozygous71151479
4133998609133998610TC44GENIChomozygous71151482
4133998646133998647CT48GENIChomozygous71151485
4133998648133998649GA49GENIChomozygous71151488
4133998681133998682GA52GENIChomozygous71151491
4133998692133998693TC57GENIChomozygous71151494
4133998742133998743GC46GENIChomozygous71151497
4133998818133998819AG34GENIChomozygous71151503
4133998917133998918AC26GENIChomozygous71151506
4133998994133998995TC35GENIChomozygous71151509
4133999440133999441CT14GENIChomozygous71151512