chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45191670051916701AG32GENIChomozygous56889848
45191687751916878AG34GENIChomozygous56889850
45191712551917126AT27GENIChomozygous56889852
45191713851917139TA25GENIChomozygous56889854
45191877051918771A-31GENIChomozygous56889856
45191964651919661ATCAATCTATCTATC---------------7GENIChomozygous58333913
45191967951919680CCT20GENICpossibly homozygous56889862
45192111451921115TC26GENIChomozygous57472457
45192112151921122CCCA26GENIChomozygous56889864
45192174251921743CT27GENIChomozygous56889866
45192181751921818T-25GENIChomozygous56889868
45192206351922064AC16GENIChomozygous56889870
45192216751922168TC20GENIChomozygous56889872
45192220651922207CT18GENIChomozygous56889874
45192222951922231AA--20GENIChomozygous56889876
45192325751923263CATACA------2GENIChomozygous58333915
45192374351923744CG30GENIChomozygous56889882
45192413351924134GA30GENIChomozygous56889884
45192529651925297TC31GENIChomozygous56889886
45192567851925679GA15GENIChomozygous56889888
45192618051926181TTA38GENIChomozygous56889890
45192644551926446GA32GENIChomozygous56889892
45192671151926712TA41GENIChomozygous56889894
45192685551926856TC32GENIChomozygous56889896
45192868151928682GA34GENIChomozygous56889898
45192873151928732TC28GENIChomozygous56889900
45192927851929279CT34GENIChomozygous56889902
45193091651930917TTACACACACACACAC17GENIChomozygous58333916
45193159851931599TG25GENIChomozygous56889904
45193213351932134CCA30GENIChomozygous56889906
45193268151932682TC15GENIChomozygous56889910
45193269851932700TT--4GENIChomozygous56889912
45193292551932933AGGAAGGC--------1GENIChomozygous56889914
45193294451932945CA1GENIChomozygous56889918
45193348851933491TTT---6GENIChomozygous56889924
45193424451934245AG30GENIChomozygous56889928
45193431951934320CT22GENIChomozygous56889930
45193432951934330GT20GENIChomozygous56889932
45193504451935045AAT22GENIChomozygous56889934
45193512751935128AC24GENIChomozygous56889936
45193517451935175TTTA15GENIChomozygous56889938