chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157683346157683347TC55GENIChomozygous112906898
4157685548157685548TCCGTCCGTCCGTCCATCCA39GENIChomozygous131364161
4157690378157690379AG44GENIChomozygous112906906
4157692682157692683CG52GENIChomozygous113400724
4157687125157687126CT28GENICpossibly homozygous113400714
4157688718157688719CT52GENIChomozygous113400716
4157689146157689147TC49GENIChomozygous113400718
4157690306157690307TC49GENICpossibly homozygous113400720
4157690573157690574GA46GENIChomozygous113400722
4157688614157688614T62GENIChomozygous128096227
4157693342157693343GA63GENIChomozygous113400726
4157693884157693885CT62GENIChomozygous113400728
4157695076157695077CT57GENIChomozygous113400730
4157698151157698152GA40GENIChomozygous113400732
4157701545157701546CT47GENIChomozygous113400734
4157705347157705348AG43GENIChomozygous113184586