chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108859994988599950GA52GENICpossibly homozygous116674231
108860056788600568GA37GENIChomozygous116901722
108860422688604227TA30GENIChomozygous116901724
108860477088604771AC41GENIChomozygous116901726
108860597788605978CG33GENIChomozygous116901728
108860753688607537TA28GENIChomozygous116901730
108860837988608380GA53GENIChomozygous116901732
108860864988608650CT48GENIChomozygous116901734
108860920188609202CG47GENICpossibly homozygous116901736
108860966688609667GA46GENIChomozygous116901738
108860977588609776CT46GENIChomozygous116901740
108860643688606437CT80GENICheterozygous118007414
108860521488605215CT13GENIChomozygous117068381
108860581388605814CA21GENICpossibly homozygous118007413