chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140092823140092824GA29GENIChomozygous112855961
4140094704140094705AC14GENIChomozygous112855965
4140096159140096160TG29GENIChomozygous113562485
4140096511140096512AG6GENIChomozygous113174952
4140096580140096581TC14GENIChomozygous119281275
4140096581140096582CT14GENIChomozygous119281277
4140096747140096748CA25GENIChomozygous112855973
4140097343140097344TG12GENIChomozygous112855975
4140097430140097431TC12GENIChomozygous112855977
4140097798140097799CT30GENIChomozygous113174954
4140097894140097895TC22GENIChomozygous113174956
4140098117140098118GA23GENIChomozygous113174958
4140098128140098129GA24GENIChomozygous113174960
4140098151140098152AG16GENIChomozygous113174962
4140098174140098175TC21GENIChomozygous113174966
4140098270140098271AC31GENIChomozygous112855979
4140098857140098858AC19GENIChomozygous113174968
4140098894140098895TA19GENIChomozygous112855993
4140099160140099161TC23GENIChomozygous112855999
4140099346140099347AG25GENIChomozygous112856007
4140100066140100067AG11GENIChomozygous112856009
4140100962140100963GC18GENIChomozygous113174970
4140101242140101243AG35GENIChomozygous112856013
4140102195140102196GA26GENIChomozygous113562488
4140103075140103076CA34GENIChomozygous113174972
4140103286140103287GT41GENIChomozygous113174974
4140103444140103445AC26GENIChomozygous113174976
4140103475140103476TC22GENIChomozygous113174978
4140104034140104035CT26GENIChomozygous113174980