chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122993378829933789TC16GENICpossibly homozygous115303238
122993382729933828AG18GENICpossibly homozygous115303240
122993386729933868CT16GENIChomozygous115303242
122993570229935703GA29GENICpossibly homozygous115601704
122993726829937269CT27GENIChomozygous115601706
122993727229937273AT26GENIChomozygous115601708
122993740829937409GA24GENICpossibly homozygous115303250
122994007129940072AG26GENICpossibly homozygous115561729
122994263029942631GA30GENICpossibly homozygous115601712
122994788229947883TC34GENICpossibly homozygous115303260
122994848829948489GA14GENICpossibly homozygous115561731
122995172229951723AC28GENICpossibly homozygous115303278
122995496229954963AG40GENICpossibly homozygous115681081
122995388029953881AG27GENIChomozygous115681071
122995388129953882TC26GENIChomozygous115681073
122995401929954020GA38GENICpossibly homozygous115681075
122995405029954051GA25GENICpossibly homozygous115681077
122995488429954885GC38GENICpossibly homozygous115681079
122995512929955130AG30GENIChomozygous115681083
122995528429955285TC30GENICpossibly homozygous115601714
122995560529955606TC10GENICpossibly homozygous115681085
122995580729955808GA21GENIChomozygous115681087
122995608629956087AT25GENICpossibly homozygous115601716