chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263449011263449012GT23GENIChomozygous109027024
1263449595263449596TA21GENIChomozygous109027025
1263450387263450388AG14GENIChomozygous108633075
1263451566263451567AG18GENIChomozygous109027026
1263452150263452151TG20GENIChomozygous109027027
1263453135263453136AG12GENIChomozygous108633083
1263455081263455082GA20GENIChomozygous109027030
1263455588263455589AT24GENIChomozygous108633087
1263455726263455727AG26GENIChomozygous109027031
1263456087263456088CT3GENIChomozygous109058139
1263457421263457422CA31GENICpossibly homozygous109027038
1263457693263457694GA19GENIChomozygous109027039
1263458131263458132TG17GENIChomozygous108633093
1263459229263459230GA24GENIChomozygous108633095
1263459234263459235GC23GENIChomozygous108633097