chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17874023378740234GT7GENIChomozygous120778421
17874171678741717TG27GENIChomozygous108873031
17874466478744665AG40GENIChomozygous120778422
17874494878744949GC21GENIChomozygous120778423
17874620878746209TG33GENIChomozygous120778424
17874627878746279GA30GENIChomozygous120778425
17874665478746655GA26GENIChomozygous108873034
17874714778747148TG35GENIChomozygous108873035
17874816178748162TC30GENIChomozygous108873036
17874839278748393TC33GENIChomozygous108873037
17874866378748664TC37GENIChomozygous108873039
17874920078749201TC25GENIChomozygous108873040
17875060678750607CT35GENIChomozygous120778426
17875066578750666TC31GENIChomozygous120778427
17875110678751107CT41GENIChomozygous120778428
17875294778752948GA38GENIChomozygous120778429
17875300278753003GT32GENICpossibly homozygous120778430
17875607378756074CT33GENICpossibly homozygous120778431
17875671378756714CT44GENIChomozygous120778432
17875693278756933TA38GENIChomozygous120778433
17875733178757332AG18GENIChomozygous108873047
17875760478757605TC36GENIChomozygous120778434
17875848378758484GA24GENIChomozygous120778435
17875925778759258AG32GENIChomozygous108873050
17875936178759362CA19GENIChomozygous120778436
17876130378761304GA18GENIChomozygous120778437
17876227478762275AG26GENIChomozygous120778438
17876375978763760TC46GENIChomozygous108873054
17876436478764365AT38GENIChomozygous120778439
17876510078765101CT37GENIChomozygous120778440