chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32211440822114409TC15GENIChomozygous148157415
32211841722118418AG21GENIChomozygous145400078
32211934022119341GA11GENIChomozygous148157416
32212161622121617CT6GENIChomozygous148157417
32212248122122482TA13GENIChomozygous148157418
32212299422122995CA16GENIChomozygous148157419
32212480822124809TC14GENIChomozygous145400080
32212617622126177CT15GENIChomozygous148157420
32212788022127881GA15GENIChomozygous148157421
32212811322128114TA17GENICpossibly homozygous145400081
32212966922129670GA12GENIChomozygous148157422
32213086022130861GC12GENIChomozygous148157423
32213134922131350CT16GENIChomozygous148157424
32213185922131860CT16GENIChomozygous148157425
32213615022136151TA28GENIChomozygous148157426
32213813222138133T11GENIChomozygous145390167
32213868622138687TC16GENIChomozygous145400087
32214016222140163AG23GENIChomozygous145400088
32214078322140784CG21GENIChomozygous145400090
32214098222140983CT27GENIChomozygous148157427
32212131322121314A24GENIChomozygous148154324
32214330522143306C14GENIChomozygous145390168
32212353422123534A16GENIChomozygous148154325
32212697522126975A12GENIChomozygous148154326
32213459922134599T17GENIChomozygous148154327
32213872422138725C19GENIChomozygous148154328
32212131322121314AG24GENICheterozygous403924005