chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51935927019359271CA10GENIChomozygous954920890
51935958619359587GA5GENIChomozygous954920891
51935999619359997AG12GENIChomozygous954920892
51936108219361083CT22GENIChomozygous954920893
51936112819361129AG23GENICpossibly homozygous954920894
51936119319361194GC18GENIChomozygous954920895
51936128019361281GC24GENIChomozygous954920896
51936208719362088CT16GENIChomozygous954920897
51936235319362354CT21GENIChomozygous954920898
51936237119362372AC16GENIChomozygous954920899
51936241619362417TG9GENIChomozygous954920900
51936251219362513GA15GENIChomozygous954920901
51936265519362656AG25GENIChomozygous954920902
51936269719362698CT27GENIChomozygous954920903
51936271819362719TC25GENIChomozygous954920904
51936286919362870CG33GENIChomozygous954920905
51936315419363155AC6GENIChomozygous954920906
51936319919363200GA7GENIChomozygous954920907
51936360719363608AG29GENIChomozygous954920908
51936466519364666GA20GENIChomozygous954920909
51936471419364715TC25GENIChomozygous954920910
51936474219364743AG29GENIChomozygous954920911
51936499819364999GA30GENIChomozygous954920912
51936529819365299GA23GENIChomozygous954920913
51936796319367964TC27GENIChomozygous954920914
51936829319368294TC20GENIChomozygous954920915