chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137025966370259664TC31GENIChomozygous795533098
137026731570267316CT35GENIChomozygous795533099
137026814470268145GA39GENIChomozygous795533100
137026850270268503CA49GENIChomozygous795533101
137027172870271729TC20GENIChomozygous795533102
137027185070271851TC37GENIChomozygous795533103
137027550870275509AT75GENICpossibly homozygous795533104
137027600370276004GA43GENIChomozygous795533105
137027612970276130TC45GENIChomozygous795533106
137027954770279548TC56GENIChomozygous795533107
137028235070282351CG37GENIChomozygous795533108
137028476270284763CT61GENIChomozygous795533109
137029326670293267CT53GENIChomozygous795533110
137029651570296516CT39GENIChomozygous795533111
137029804070298041AG21GENICpossibly homozygous795533112
137029805270298053AT17GENICpossibly homozygous795533113
137030117070301171CG18GENICpossibly homozygous795533114
137030672170306722TC53GENIChomozygous795533115