chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109613199996132000AC16GENICpossibly homozygous118051571
109613666196136662AG35GENIChomozygous116689375
109614313496143135CT2GENIChomozygous118051580
109614313896143139CT2GENIChomozygous118051582
109614314296143143GT2GENIChomozygous118051584
109614314696143147GT2GENIChomozygous118051586
109614315096143151CT3GENIChomozygous118051587
109614315496143155GT3GENIChomozygous118009793
109614316696143167CT20GENIChomozygous118009794
109615865796158658AT28GENICheterozygous118009795
109615965696159657AT25GENICheterozygous118051589
109616232796162328GC32GENIChomozygous118051591
109616386696163867GT10GENIChomozygous118051592
109616387096163871CT10GENIChomozygous118051594
109616387196163872AG10GENIChomozygous118051596