chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105600116856001168A13GENICheterozygous130392704
105600164656001647T21GENIChomozygous131094408
105600866156008662GC11GENIChomozygous123362779
105600882356008823C19GENIChomozygous128819079
105600855756008558AG23GENIChomozygous116602946
105600856056008561GC23GENIChomozygous116602948
105600877656008777GC18GENIChomozygous116602950
105600862156008621T15GENIChomozygous128819073
105600862656008627C14GENIChomozygous128819074
105600866356008668GTGGC11GENIChomozygous128819075
105600867756008677GT11GENIChomozygous128819076
105600871756008717G11GENIChomozygous128819077
105600873656008737C12GENIChomozygous128819078
105600868056008681TG11GENIChomozygous116978038
105600885056008850T20GENIChomozygous128819080
105600888656008887A18GENIChomozygous128819081
105600889756008899AG15GENIChomozygous128819082