chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4102805942102805943CG74GENIChomozygous137184552
4102810901102810902AG35GENIChomozygous143134966
4102813002102813003AC52GENIChomozygous137184553
4102817451102817452GT35GENICpossibly homozygous137184554
4102818000102818001CG57GENIChomozygous137184555
4102818001102818002TA56GENIChomozygous137184556
4102827979102827980AT45GENIChomozygous137184557
4102827980102827981GT45GENIChomozygous137184558
4102828445102828446CT48GENIChomozygous137184559
4102829786102829787TC64GENIChomozygous137184560
4102830337102830337T49GENICpossibly homozygous136908600
4102817879102817879TAAAAAT46GENIChomozygous136908596
4102823633102823633TGT59GENIChomozygous136908597
4102828009102828009C44GENIChomozygous136908598
4102828565102828565TCCCTGCAG44GENIChomozygous136908599
4102831346102831347AG49GENIChomozygous137184561
4102832683102832684AT20GENIChomozygous137184562
4102832771102832772AG35GENIChomozygous137184563
4102835603102835604AG52GENIChomozygous137184564
4102835661102835662CT52GENIChomozygous137184565
4102835754102835755CT55GENIChomozygous137184566
4102837349102837350CT56GENIChomozygous137184567
4102837712102837713CG58GENIChomozygous137184568
4102841861102841862CT50GENIChomozygous137184569
4102842684102842685CT51GENIChomozygous137184570
4102843743102843744GT68GENIChomozygous137184571
4102850230102850231CT55GENIChomozygous137184572
4102855199102855200TC48GENICpossibly homozygous137184573
4102857689102857690GA51GENIChomozygous137184575
4102858892102858893GA51GENIChomozygous137184576
4102861868102861869GT51GENIChomozygous137184577
4102866584102866585AG45GENIChomozygous137184578