chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105873359858733599TG35GENIChomozygous116606930
105873498158734982AT51GENIChomozygous116606946
105873524658735247AC40GENICpossibly homozygous116606948
105874728958747290TC29GENIChomozygous116607022
105874996258749963AG27GENIChomozygous116607032
105875310958753110AT40GENICpossibly homozygous116787831
105875366758753668AG35GENIChomozygous116607044
105875564058755641AT55GENIChomozygous116607048
105875696458756965AG37GENIChomozygous116607050
105876135758761358GA67GENIChomozygous116607052
105876170958761710TC47GENICpossibly homozygous117079379
105873942958739430CT35GENIChomozygous117079372
105875740658757407CT34GENIChomozygous117079373
105875848058758481TG30GENIChomozygous117079375
105875979358759794GA43GENIChomozygous117079376
105876154358761544GA56GENIChomozygous117079378
105875550758755508AT36GENIChomozygous117411086
105875638958756390GA49GENICheterozygous118083741
105876193958761940GA31GENIChomozygous117079381
105876195358761954AG34GENIChomozygous116607056
105876269858762699AC29GENIChomozygous117079382
105876879558768796GT58GENIChomozygous116607064
105876983358769834GA23GENIChomozygous116607068
105877055358770554GA41GENIChomozygous117079383
105877063258770633GA34GENIChomozygous117079385
105877204858772049TG41GENIChomozygous116787919
105877392658773927AG42GENIChomozygous116607074
105877403358774034AG36GENIChomozygous116607076
105877453258774533CA25GENIChomozygous117079386
105877548258775483CT35GENICpossibly homozygous117104108
105877561958775620GT41GENIChomozygous118083742
105877562058775621CA41GENICpossibly homozygous118083743
105877649558776496CT34GENIChomozygous116937084