chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
23184118731841188AG18GENIChomozygous145354654
23184215631842157TG20GENIChomozygous145354655
23184509331845094GA12GENICpossibly homozygous145354656
23184575031845751CT9GENIChomozygous145354657
23184849731848498AG20GENIChomozygous140972061
23184899731848998GA24GENIChomozygous140972063
23184939131849392AC17GENIChomozygous140972064
23184949331849494TC23GENIChomozygous140972065
23185042831850429AG13GENIChomozygous140972066
23185199831851999TC7GENIChomozygous140972068
23185373131853732GA15GENIChomozygous140972075
23185411031854111GT16GENIChomozygous145354658
23185413631854137CT16GENIChomozygous140972078
23185426631854267CG17GENIChomozygous145354659
23185429531854296CT19GENIChomozygous145354660
23185435831854359AT12GENIChomozygous140972080
23185436731854368TA11GENIChomozygous140972081
23185471931854720CT10GENIChomozygous145354661
23185604731856048AG17GENIChomozygous145354662
23185683131856832G18GENICpossibly homozygous140967184
23184600831846010GA24GENIChomozygous145342443
23184632231846339GGGTGATGGTGTCTTGG15GENIChomozygous142893243
23185440031854401A11GENIChomozygous140967180
23185628731856287TAAG25GENIChomozygous140967183
23185702431857025A18GENIChomozygous145342444
23185733431857335AG16GENIChomozygous140972092
23185776531857766CT24GENIChomozygous145354663
23185834631858346CTTTCTTTCTTTCTTTCTTC14GENIChomozygous140967185
23185955031859551GA24GENIChomozygous140972101
23186056731860568AG15GENIChomozygous140972103
23186064431860645GA26GENIChomozygous145354664
23186083531860836GA26GENIChomozygous145354665
23186102231861023AG18GENIChomozygous140972105
23186143731861438T14GENIChomozygous145342445
23186175431861755C8GENIChomozygous145342446
23186277931862780CT19GENIChomozygous145354666
23186283631862837TC23GENIChomozygous145354667
23186308931863090TG18GENIChomozygous145354668
23186354631863547AG22GENIChomozygous140972110
23186383731863838GA24GENIChomozygous140972112
23186465231864653GC17GENIChomozygous142930521