chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187478772974787730GT11GENICpossibly homozygous63940491
187479790674797907TG12GENIChomozygous64068047
187479790774797908GT12GENIChomozygous64068048
187479840974798410AC4GENIChomozygous63940493
187479846874798469GT7GENIChomozygous63940495
187492977774929778TA15GENIChomozygous64068052
187493753774937538TC24GENICheterozygous63940531
187493753974937540TC26GENICheterozygous63940533
187493970774939708TC1GENIChomozygous63940555
187493971374939714GC1GENIChomozygous63940557
187493972974939730GT1GENIChomozygous63940559
187493975374939754AC2GENIChomozygous63940567
187493975474939755GT2GENIChomozygous63940569