chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142410380024103801TG16INTERGENIChomozygous804607671
142410420124104202CG11GENIChomozygous804607672
142410443224104433GT15GENIChomozygous804607673
142410444624104447GA15GENICpossibly homozygous804607674
142410456424104565GA12GENIChomozygous804607675
142410471824104719GA14GENIChomozygous804607676
142410474224104743TC13GENIChomozygous804607677
142410545724105458TC26GENIChomozygous804607678
142410559624105597CT19GENIChomozygous804607679
142410741224107413AG9GENIChomozygous804607680
142410841524108416TC4GENIChomozygous804607681
142410878024108781AG9GENIChomozygous804607682
142410966624109667AG12GENIChomozygous804607683
142411609024116091CG10GENIChomozygous804607684
142411653724116538TC14GENIChomozygous804607685
142411943824119439TA19GENIChomozygous804607686
142411988824119889GA9GENIChomozygous804607687
142412028624120287GA13GENIChomozygous804607688
142412098624120987CT10GENIChomozygous804607689
142412105324121054TA5GENIChomozygous804607690
142412123724121238GA14GENIChomozygous804607691
142412148724121488GA14GENIChomozygous804607692
142412242224122423CT26GENICpossibly homozygous804607693
142412243424122435AG27GENICpossibly homozygous804607694
142412329224123293GT24GENIChomozygous804607695
142412331324123314GC20GENIChomozygous804607696
142412389124123892GC12GENIChomozygous804607697
142412462824124629AG17GENIChomozygous804607698
142412481524124816CT13GENIChomozygous804607699
142412524224125243TC14GENIChomozygous804607700