chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4102805942102805943CG52GENIChomozygous137184552
4102810901102810902AG50GENIChomozygous143134966
4102813002102813003AC48GENIChomozygous137184553
4102817451102817452GT34GENIChomozygous137184554
4102818000102818001CG43GENIChomozygous137184555
4102818001102818002TA42GENIChomozygous137184556
4102818545102818546AG46GENIChomozygous154235624
4102827979102827980AT30GENIChomozygous137184557
4102827980102827981GT32GENIChomozygous137184558
4102818545102818546A46GENICheterozygous144659599
4102828445102828446CT42GENIChomozygous137184559
4102828565102828565TCCCTGCAG40GENIChomozygous136908599
4102828009102828009C36GENIChomozygous136908598
4102817879102817879TAAAAAT36GENIChomozygous136908596
4102823633102823633TGT38GENIChomozygous136908597
4102821828102821829C17GENIChomozygous403116364
4102821828102821829CA17GENICheterozygous403116365
4102829786102829787TC53GENIChomozygous137184560
4102830337102830337T43GENICpossibly homozygous136908600
4102831346102831347AG46GENIChomozygous137184561
4102832675102832676T14GENICheterozygous147973475
4102832675102832676TC14GENIChomozygous154235626
4102832683102832684AT16GENIChomozygous137184562
4102832771102832772AG35GENIChomozygous137184563
4102835603102835604AG45GENIChomozygous137184564
4102835661102835662CT45GENIChomozygous137184565
4102835754102835755CT37GENIChomozygous137184566
4102837349102837350CT44GENIChomozygous137184567
4102837712102837713CG47GENIChomozygous137184568
4102841861102841862CT41GENIChomozygous137184569
4102842684102842685CT41GENIChomozygous137184570
4102861868102861869GT42GENIChomozygous137184577
4102843743102843744GT35GENIChomozygous137184571
4102850230102850231CT47GENIChomozygous137184572
4102855199102855200TC37GENIChomozygous137184573
4102857689102857690GA41GENIChomozygous137184575
4102858892102858893GA31GENIChomozygous137184576
4102866584102866585AG50GENIChomozygous137184578