chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142410420124104202CG30GENIChomozygous800252676
142410443224104433GT15GENIChomozygous800252677
142410444624104447GA18GENIChomozygous800252678
142410456424104565GA24GENIChomozygous800252679
142410471824104719GA18GENIChomozygous800252680
142410474224104743TC19GENIChomozygous800252681
142410545724105458TC40GENIChomozygous800252682
142410559624105597CT35GENIChomozygous800252683
142410701424107015CG16GENIChomozygous800252684
142410741224107413AG21GENIChomozygous800252685
142410841524108416TC11GENIChomozygous800252686
142410860124108602CA5GENIChomozygous800252687
142410878024108781AG6GENIChomozygous800252688
142410966624109667AG19GENIChomozygous800252689
142411609024116091CG13GENIChomozygous800252690
142411653724116538TC13GENIChomozygous800252691
142411943824119439TA20GENIChomozygous800252692
142411988824119889GA23GENIChomozygous800252693
142412028624120287GA21GENIChomozygous800252694
142412098624120987CT28GENIChomozygous800252695
142412105324121054TA41GENIChomozygous800252696
142412123724121238GA20GENIChomozygous800252697
142412148724121488GA22GENIChomozygous800252698
142412242224122423CT36GENICpossibly homozygous800252699
142412243424122435AG33GENICpossibly homozygous800252700
142412329224123293GT22GENIChomozygous800252701
142412331324123314GC22GENICpossibly homozygous800252702
142412389124123892GC30GENIChomozygous800252703
142412462824124629AG18GENIChomozygous800252704
142412481524124816CT20GENIChomozygous800252705
142412524224125243TC27GENIChomozygous800252706