chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141525382415253825GT21GENIChomozygous113356604
141525383415253835GA22GENIChomozygous113356606
141525397515253976CT24GENIChomozygous113356608
141525483615254837G16GENIChomozygous129127877
141525485315254854GT12GENIChomozygous113356610
141525493915254940TA22GENIChomozygous113356612
141525497015254971TC21GENIChomozygous113356614
141525574215255743CT18GENIChomozygous113356616
141525576715255768GA17GENIChomozygous113356618
141525578415255785GA17GENIChomozygous113356620
141525593515255936TG16GENIChomozygous113356622
141525599515255996CG22GENIChomozygous113356624
141525620715256208GC16GENIChomozygous113356626
141525665015256651GT17GENIChomozygous113356628
141525722515257226TC14GENIChomozygous113356630
141525761715257617CATCTTGC16GENIChomozygous129127878
141525791415257914A18GENIChomozygous129127879