chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103781401737814018GA10GENIChomozygous51419649
103781407137814072AG7GENIChomozygous51419651
103781407737814078CA10GENIChomozygous51419653
103781410237814103AT12GENIChomozygous51419655
103781516637815167TC12GENICheterozygous51419657
103781529837815299TC15GENIChomozygous51419659
103781539037815391GA23GENICpossibly homozygous51419661
103781543737815438TC15GENIChomozygous51419663
103781564137815649CACACACA--------2GENIChomozygous51419669
103781696037816961TC26GENIChomozygous51419673
103781746937817470T-5GENIChomozygous51419675
103781764937817650TC13GENIChomozygous51419677
103781804937818050AT10GENIChomozygous51419679
103781805037818051AC10GENIChomozygous51419681
103781865237818653AT21GENIChomozygous51419685
103781951137819512TC25GENIChomozygous51419687
103781960337819604G-15GENIChomozygous51419689
103782137837821379GA14GENIChomozygous51419691
103782187737821878CA20GENIChomozygous51419693
103782208837822089AG19GENICpossibly homozygous51419695
103782210737822108AAACACACACACACACACACAC1GENIChomozygous52316340
103782244737822448GA18GENIChomozygous51419703
103782261337822614TC12GENIChomozygous51419704
103782276437822765TTA2GENIChomozygous51419706
103782300037823001TTG7GENICpossibly homozygous51419708
103782331037823311CT27GENIChomozygous51419710
103782336737823368TC17GENICpossibly homozygous51419712
103782415037824151G-12GENIChomozygous51419716
103782438737824388TC16GENICpossibly homozygous51419718
103782447437824481TTTTTTC-------3GENICheterozygous51419720
103782494337824944GA11GENIChomozygous51419726
103782582437825825TG8GENIChomozygous51419728
103782642837826429TC24GENICpossibly homozygous51419730
103782672737826728CT21GENIChomozygous51419732
103782689637826897CT13GENIChomozygous51419734
103782689737826898TG13GENIChomozygous51419736
103782700437827005GA19GENIChomozygous51419738
103782712837827129CA11GENICpossibly homozygous51419740