chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187478772974787730GT18GENICpossibly homozygous63940491
187479790674797907TG18GENICpossibly homozygous64068047
187479790774797908GT18GENICpossibly homozygous64068048
187479840974798410AC9GENIChomozygous63940493
187479846874798469GT6GENICheterozygous63940495
187492977774929778TA11GENIChomozygous64068052
187493753774937538TC16GENICheterozygous63940531
187493753974937540TC17GENICheterozygous63940533
187493970774939708TC2GENIChomozygous63940555
187493971374939714GC2GENIChomozygous63940557
187493972974939730GT2GENIChomozygous63940559
187493973974939740TC2GENIChomozygous63940561
187493974174939742GC2GENIChomozygous63940563
187493974774939748CA1GENIChomozygous63940565
187493975374939754AC1GENIChomozygous63940567
187493975474939755GT1GENIChomozygous63940569