chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4146924200146924201AG10GENIChomozygous112873747
4146925608146925609CT16GENIChomozygous113180088
4146925748146925749AT25GENIChomozygous113180089
4146926747146926748CT26GENIChomozygous113180090
4146926799146926800TC26GENIChomozygous113180091
4146927088146927089AG19GENIChomozygous112873749
4146927799146927800GA23GENIChomozygous113180092
4146928535146928536CA17GENIChomozygous113180093
4146928578146928579TC13GENIChomozygous113180094
4146928922146928923AG13GENIChomozygous112873750
4146929064146929065GA9GENIChomozygous113180095
4146930568146930569TC30GENIChomozygous112873752
4146932544146932545TC21GENIChomozygous112873754
4146932641146932642CT15GENIChomozygous112873755
4146933680146933681TC17GENIChomozygous112873756
4146933976146933977AC24GENIChomozygous113180097
4146934115146934116TG21GENIChomozygous112873757
4146937576146937577GA21GENIChomozygous113180098
4146938480146938481GA33GENIChomozygous112873763
4146938488146938489TC34GENIChomozygous112873764
4146940011146940012TC23GENIChomozygous113180099
4146940389146940390GA32GENIChomozygous113180100
4146940682146940683TC28GENIChomozygous112873765
4146944814146944815TC20GENIChomozygous113180102
4146944849146944850CT16GENIChomozygous113180103
4146945741146945742GA19GENIChomozygous113180104
4146946058146946059TC26GENIChomozygous113180105
4146946272146946273AG16GENIChomozygous113180106
4146946408146946409CT15GENIChomozygous112873771
4146946875146946876CT19GENIChomozygous113180108
4146947778146947779TC19GENIChomozygous113180109
4146948720146948721GA26GENIChomozygous113180110
4146948970146948971AG23GENIChomozygous113180111