chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140092823140092824GA24GENIChomozygous112855961
4140094704140094705AC20GENIChomozygous112855965
4140094831140094832GA15GENIChomozygous113174948
4140096159140096160TG21GENIChomozygous113562485
4140096580140096581TC9GENIChomozygous119281275
4140096581140096582CT9GENIChomozygous119281277
4140096747140096748CA16GENIChomozygous112855973
4140097343140097344TG11GENIChomozygous112855975
4140097430140097431TC10GENIChomozygous112855977
4140097798140097799CT19GENIChomozygous113174954
4140097894140097895TC24GENIChomozygous113174956
4140098117140098118GA22GENIChomozygous113174958
4140098128140098129GA23GENIChomozygous113174960
4140098151140098152AG21GENIChomozygous113174962
4140098174140098175TC26GENIChomozygous113174966
4140098270140098271AC18GENIChomozygous112855979
4140098411140098412AG24GENIChomozygous112855985
4140098434140098435CT28GENIChomozygous119281279
4140098439140098440TC28GENIChomozygous113056576
4140098451140098452TC28GENIChomozygous112855987
4140098481140098482GA24GENIChomozygous113562486
4140098857140098858AC25GENIChomozygous113174968
4140098894140098895TA22GENIChomozygous112855993
4140099160140099161TC17GENIChomozygous112855999
4140099346140099347AG25GENIChomozygous112856007
4140100066140100067AG11GENIChomozygous112856009
4140100962140100963GC23GENIChomozygous113174970
4140101242140101243AG28GENIChomozygous112856013
4140103075140103076CA29GENIChomozygous113174972
4140103286140103287GT24GENIChomozygous113174974
4140103444140103445AC26GENIChomozygous113174976
4140103475140103476TC25GENIChomozygous113174978