chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182470976824709769GA29GENIChomozygous110831879
182471000324710004GC22GENIChomozygous110831881
182471117424711175CA2GENIChomozygous110831883
182471266624712667GA28GENIChomozygous110831885
182471385924713860GA25GENIChomozygous110831887
182471520424715205GA12GENIChomozygous110309057
182471569824715699TC43GENIChomozygous110309059
182471603824716039CA20GENIChomozygous110309061
182471720024717201CT28GENIChomozygous110831889
182471731024717311GA34GENIChomozygous110831892
182471771224717713GC30GENIChomozygous110831894
182472100024721001AG12GENIChomozygous110309065
182472246624722467AG23GENIChomozygous110309067
182472293324722934TG22GENIChomozygous110831896
182472293724722938TG22GENIChomozygous110831898
182472462024724621TG20GENIChomozygous110647494
182472664624726647TC13GENIChomozygous110831900
182472860624728607GA26GENIChomozygous110831902
182472905424729055AG25GENIChomozygous110309069
182473241424732415TC38GENIChomozygous110309073
182473264624732647AG28GENIChomozygous110309075
182473281924732820AG23GENIChomozygous110309077
182473328624733287GA28GENIChomozygous110309081
182473520324735204GA30GENIChomozygous110309085
182473587024735871AG21GENIChomozygous110309087
182473616724736168CT29GENIChomozygous110309089
182473668724736688TC23GENIChomozygous110309091
182474030224740303AT24GENIChomozygous110309093
182474129524741296CT19GENIChomozygous110309095
182474296424742965TA32GENIChomozygous110309097
182474485124744852CT30GENIChomozygous110309099
182474553424745535CT29GENIChomozygous110309103