chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108859994988599950GA57GENIChomozygous116674231
108859995288599953A54GENIChomozygous128843430
108860521488605215CT28GENIChomozygous117068381
108860674888606749T43GENICpossibly homozygous131468813
108860710288607103A38GENIChomozygous131468814
108860753688607537TA43GENIChomozygous116901730
108860056788600568GA54GENIChomozygous116901722
108860422688604227TA48GENIChomozygous116901724
108860477088604771AC44GENIChomozygous116901726
108860597788605978CG45GENIChomozygous116901728
108860581388605814CA16GENIChomozygous118007413
108860837988608380GA64GENIChomozygous116901732
108860864988608650CT37GENIChomozygous116901734
108860872888608730GC43GENIChomozygous131468815
108860912188609123AA39GENIChomozygous131468816
108860920188609202CG36GENIChomozygous116901736
108860966688609667GA46GENIChomozygous116901738
108860977588609776CT35GENIChomozygous116901740