chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6102032297102032298GA16GENICpossibly homozygous114919135
6102032524102032525AG17GENIChomozygous114919136
6102032684102032685TC20GENIChomozygous114919137
6102032794102032795AG23GENIChomozygous114919138
6102033111102033112AG28GENIChomozygous114919140
6102035028102035029CT23GENIChomozygous115411439
6102035697102035698CT21GENIChomozygous114919141
6102039637102039638CT15GENIChomozygous114919142
6102041318102041319GA16GENIChomozygous114919143
6102042493102042494TC26GENIChomozygous114919145
6102044371102044372GA14GENIChomozygous115411440
6102045646102045647GC20GENIChomozygous114919147
6102046598102046599GA32GENIChomozygous114919148