chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123920915639209157CA8GENICpossibly homozygous115325054
123920980339209804GA23GENIChomozygous115325056
123920988939209890AT31GENIChomozygous115325058
123921042139210422CT30GENIChomozygous115325060
123921121739211218CT26GENIChomozygous115325062
123921297939212980TG12GENIChomozygous115325064
123921333139213332GA5GENIChomozygous115325068
123921644939216450GT24GENIChomozygous115325070
123921747039217471AG27GENIChomozygous115325072
123921858839218589TC25GENIChomozygous115325074
123922127539221276AG33GENIChomozygous115325076
123922134639221347CT30GENIChomozygous115325078
123922194139221942AG20GENIChomozygous115325080
123922279339222794AC11GENIChomozygous115325082
123922296839222969AG17GENIChomozygous115325084
123922297339222974CT15GENIChomozygous115325086
123922522039225221GA21GENIChomozygous115325092
123922556539225566AC21GENIChomozygous115325096
123922580739225808TC29GENIChomozygous115325098
123922639339226394GT30GENIChomozygous115325102
123922921739229218AG28GENIChomozygous115325104
123922947439229475GA20GENIChomozygous115325106
123922963139229632TG20GENIChomozygous115325108
123923048739230488TA18GENIChomozygous115325110
123923290939232910CT11GENIChomozygous115383209
123923512339235124CT19GENIChomozygous115325112
123923551739235518TC16GENIChomozygous115325114
123923581939235820AG16GENIChomozygous115325116
123923676239236763GA29GENIChomozygous115325118
123923806239238063AG23GENIChomozygous115325120
123923807139238072AG22GENIChomozygous115325122
123923833039238331TC23GENIChomozygous115325124
123924070839240709GA29GENIChomozygous115325126
123924184939241850AT25GENIChomozygous115325128
123924186339241864CT25GENIChomozygous115325130
123924201239242013CT23GENIChomozygous115325132