chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108498655384986554CT18GENIChomozygous116814736
108498669384986694CT8GENIChomozygous117018696
108498779084987791TC31GENIChomozygous116814738
108498874084988741GA37GENIChomozygous116814740
108498925884989259CT26GENIChomozygous117018697
108498950284989503AG23GENIChomozygous116814742
108499033584990336GT27GENIChomozygous117018698
108499052384990524GA29GENIChomozygous117018699
108499082884990829TA24GENIChomozygous117018700
108499082984990830CT25GENIChomozygous117018701
108499170384991704GA29GENIChomozygous117018702
108499232984992330AG18GENIChomozygous116814756
108499242084992421TC41GENIChomozygous116814758
108499267784992678GC24GENIChomozygous117018703
108499311884993119GC25GENIChomozygous116814760
108499321084993211TA32GENIChomozygous116814762
108499337784993378GA34GENIChomozygous117018704
108499391584993916TC14GENIChomozygous116814764
108499398184993982GC18GENIChomozygous117018705
108499399984994000TC16GENIChomozygous116814766
108499407284994073TA21GENIChomozygous116814768
108499410084994101CT14GENIChomozygous116814770
108499421984994220AG27GENIChomozygous116814772
108499423084994231TC26GENIChomozygous116814774
108499505184995052CT19GENIChomozygous116814776
108499548884995489AG23GENIChomozygous116814778
108499702884997029GC20GENIChomozygous117018706
108499818184998182GA22GENIChomozygous117018707
108499848784998488AG24GENIChomozygous117018708
108499885084998851AG32GENIChomozygous117018709
108500028685000287GC20GENIChomozygous117018710