chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31393701113937012AG28GENIChomozygous111452046
31393718513937186GA23GENIChomozygous111878816
31393731713937318AG11GENIChomozygous111452047
31393750413937505TC7GENIChomozygous111878818
31393770213937703TC13GENIChomozygous111452048
31393817013938171GA18GENIChomozygous111878822
31393832213938323GA22GENIChomozygous111878824
31393838113938382CT26GENICpossibly homozygous119697172
31393840113938402TC27GENIChomozygous111878826
31393853813938539AG21GENIChomozygous111878828
31393859713938598AG16GENIChomozygous111452050
31393904313939044TC25GENIChomozygous111452051
31393910013939101CT21GENIChomozygous119697173
31393973613939737AG38GENIChomozygous111878830
31393992213939923CT31GENIChomozygous111878834
31394001213940013TC26GENIChomozygous111452054
31394004913940050AG21GENIChomozygous111878836
31394040313940404GA22GENIChomozygous111878840
31394049513940496AG23GENIChomozygous111452056
31394050813940509AG23GENIChomozygous111452057
31394060013940601TC25GENIChomozygous111452058
31394412113944122GA27GENIChomozygous119697174
31394457613944577CT23GENIChomozygous111878846
31394576113945762CG33GENIChomozygous111878852
31394831613948317GA31GENIChomozygous119697175
31395328213953283AG20GENIChomozygous111452088
31395376713953768TC26GENIChomozygous111878862
31395402013954021CT18GENIChomozygous111878864
31395493913954940GT23GENIChomozygous119697177