chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187478772974787730GT19GENICpossibly homozygous63940491
187479790674797907TG18GENIChomozygous64068047
187479790774797908GT18GENIChomozygous64068048
187479840974798410AC11GENIChomozygous63940493
187479846874798469GT4GENIChomozygous63940495
187492977774929778TA12GENIChomozygous64068052
187493753774937538TC50GENICheterozygous63940531
187493753974937540TC53GENICheterozygous63940533
187493970774939708TC4GENIChomozygous63940555
187493971374939714GC5GENIChomozygous63940557
187493972974939730GT6GENIChomozygous63940559
187493973974939740TC5GENIChomozygous63940561
187493974174939742GC5GENIChomozygous63940563
187493974774939748CA6GENIChomozygous63940565
187493975374939754AC4GENIChomozygous63940567
187493975474939755GT4GENIChomozygous63940569