chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1168442603168442604AG29GENIChomozygous135740836
1168442827168442828GA21GENIChomozygous135740837
1168442904168442905T28GENIChomozygous135443827
1168443546168443547TC23GENIChomozygous135740838
1168443593168443594TC24GENIChomozygous135740839
1168444558168444559GA17GENICpossibly homozygous135740840
1168445705168445706TC24GENIChomozygous135740841
1168445823168445824AG17GENIChomozygous135740842
1168446243168446244AG32GENIChomozygous135740843
1168447525168447526TC26GENIChomozygous135740844
1168447614168447615CT27GENIChomozygous135740845
1168447944168447945A18GENICpossibly homozygous135443828
1168448630168448631AG22GENIChomozygous135740846
1168450555168450556GA20GENIChomozygous135740847
1168450849168450850TC9GENIChomozygous135740848
1168451087168451088AC13GENIChomozygous135740849
1168452017168452018TC30GENIChomozygous135740850
1168452606168452607TC16GENIChomozygous135740851
1168452783168452784CG23GENIChomozygous135740852
1168453160168453161CA15GENIChomozygous135740853