chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135043563750435638AC40GENIChomozygous791010601
135043624150436242GC23GENIChomozygous791010602
135043759050437591AG16GENIChomozygous791010603
135043849150438492GA12GENIChomozygous791010604
135043935250439353CT29GENIChomozygous791010605
135043976150439762TC40GENIChomozygous791010606
135044094850440949AG22GENIChomozygous791010607
135044230950442310CT30GENIChomozygous791010608
135045452750454528TC15GENIChomozygous791010609
135045551250455513CT30GENIChomozygous791010610
135045592450455925TC18GENIChomozygous791010611
135045626150456262CT22GENIChomozygous791010612
135045683450456835CT28GENIChomozygous791010613
135045712850457129AT7GENIChomozygous791010614
135045738150457382GA11GENIChomozygous791010615
135045738350457384GA10GENIChomozygous791010616
135045740750457408GA11GENIChomozygous791010617
135045788450457885CT34GENIChomozygous791010618
135045811150458112GC32GENIChomozygous791010619
135045902250459023CT24GENIChomozygous791010620
135045928450459285CG34GENIChomozygous791010621
135045929550459296CT36GENIChomozygous791010622
135045981650459817CT31GENIChomozygous791010623
135045985850459859TC28GENIChomozygous791010624
135045996750459968GA22GENIChomozygous791010625
135046014250460143GA19GENIChomozygous791010626
135046016750460168AG20GENIChomozygous791010627
135046051150460512GA14GENIChomozygous791010628
135046079550460796CT23GENIChomozygous791010629
135046082850460829CT26GENIChomozygous791010630
135046089650460897CG25GENIChomozygous791010631
135046107950461080CT26GENIChomozygous791010632
135046151050461511AT36GENIChomozygous791010633
135046162950461630GA27GENIChomozygous791010634
135046177550461776CG29GENIChomozygous791010635
135046277250462773AG26GENIChomozygous791010636
135046360050463601CT18GENIChomozygous791010637
135046362650463627AG25GENIChomozygous791010638
135046421050464211CT29GENICpossibly homozygous791010639
135046486950464870TG22GENIChomozygous791010640
135046493750464938AG25GENIChomozygous791010641
135046505550465056GA17GENIChomozygous791010642
135046527350465274GT30GENIChomozygous791010643
135046548850465489TC30GENIChomozygous791010644
135046559150465592AC30GENIChomozygous791010645
135046566250465663AG24GENIChomozygous791010646
135046587050465871TC28GENIChomozygous791010647
135046594750465948GA34GENIChomozygous791010648
135046639850466399AT12GENIChomozygous791010649
135046644450466445CG15GENIChomozygous791010650
135046664350466644AG9GENICheterozygous791010651
135046725850467259GA28GENIChomozygous791010652
135046785950467860TC38GENIChomozygous791010653
135046789550467896AG46GENIChomozygous791010654
135046817550468176AG39GENIChomozygous791010655
135046905350469054CA30GENICpossibly homozygous791010656
135047180550471806AG34GENIChomozygous791010657
135047184150471842AG34GENIChomozygous791010658
135047197950471980TC29GENIChomozygous791010659
135047340850473409TC25GENIChomozygous791010660
135047491050474911GT31GENIChomozygous791010661
135047628250476283TC40GENIChomozygous791010662
135047645850476459CT35GENIChomozygous791010663
135047836750478368GA28GENIChomozygous791010664
135047848750478488CT31GENIChomozygous791010665
135047869550478696CT32GENIChomozygous791010666
135047898150478982CT28GENIChomozygous791010667