chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108859994988599950GA62GENIChomozygous116674231
108859995288599953A59GENIChomozygous128843430
108860056788600568GA54GENIChomozygous116901722
108860422688604227TA42GENIChomozygous116901724
108860477088604771AC55GENIChomozygous116901726
108860521488605215CT28GENIChomozygous117068381
108860597788605978CG55GENIChomozygous116901728
108860674888606749T49GENICpossibly homozygous131468813
108860710288607103A52GENIChomozygous131468814
108860753688607537TA44GENIChomozygous116901730
108860837988608380GA49GENIChomozygous116901732
108860864988608650CT52GENIChomozygous116901734
108860872888608730GC42GENIChomozygous131468815
108860876088608762CT45GENICheterozygous132147096
108860912188609123AA28GENIChomozygous131468816
108860920188609202CG41GENIChomozygous116901736
108860966688609667GA44GENIChomozygous116901738
108860977588609776CT43GENIChomozygous116901740
108860581388605814CA23GENIChomozygous118007413