chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148573318985733190CT32GENICpossibly homozygous66544752
148573454185734542GT25GENICpossibly homozygous66544753
148573510085735101AG24GENICpossibly homozygous66544754
148573736585737366TC13GENICpossibly homozygous66544755
148573903685739037AG28GENICpossibly homozygous66544756
148574244485742445GA26GENICpossibly homozygous66544757
148574380585743806AC37GENICpossibly homozygous66544758
148574510285745103AG20GENICpossibly homozygous66544759
148574525185745252AC21GENICpossibly homozygous67513933
148574525685745257AG18GENICpossibly homozygous66544760
148574526485745265CT17GENIChomozygous66544761
148574575685745757CT22GENICpossibly homozygous66544762
148574636085746361TC26GENIChomozygous66544763
148574827185748272CG24GENICpossibly homozygous66544764
148574875585748756AG20GENIChomozygous66544765
148574508185745082GA24GENICpossibly homozygous67588171
148575186485751865AG20GENIChomozygous66106655
148575270385752704TC35GENIChomozygous66544766
148575401485754015TC29GENICpossibly homozygous66544767
148575586785755868GT24GENIChomozygous66544768
148575793585757936CT23GENICpossibly homozygous66544769
148575826085758261GA18GENIChomozygous66544770
148575862385758624GC10GENIChomozygous66544771