chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157683346157683347TC20GENIChomozygous112906898
4157685548157685548TCCGTCCGTCCGTCCATCCA23GENIChomozygous131364161
4157687125157687126CT9GENIChomozygous113400714
4157688614157688614T15GENIChomozygous128096227
4157688718157688719CT20GENIChomozygous113400716
4157689146157689147TC10GENIChomozygous113400718
4157690306157690307TC20GENIChomozygous113400720
4157690378157690379AG16GENIChomozygous112906906
4157690573157690574GA16GENIChomozygous113400722
4157692682157692683CG23GENIChomozygous113400724
4157693342157693343GA19GENIChomozygous113400726
4157693884157693885CT14GENIChomozygous113400728
4157695076157695077CT24GENIChomozygous113400730
4157698151157698152GA15GENIChomozygous113400732
4157701545157701546CT24GENIChomozygous113400734
4157705347157705348AG25GENIChomozygous113184586