chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142093570320935704CT13GENIChomozygous791158965
142093596520935966GA9GENIChomozygous791158966
142093635020936351GA19GENIChomozygous791158967
142093833620938337TG32GENICpossibly homozygous791158968
142093903820939039AT21GENIChomozygous791158969
142093939420939395AG22GENIChomozygous791158970
142094164320941644AG7GENIChomozygous791158971
142094166320941664GC5GENIChomozygous791158972
142094208520942086CA12GENIChomozygous791158973
142094214020942141CG14GENIChomozygous791158974
142094222920942230TC13GENIChomozygous791158975
142094223220942233CA13GENIChomozygous791158976
142094261420942615GC21GENIChomozygous791158977
142094468420944685AG15GENIChomozygous791158978
142094491220944913AG26GENIChomozygous791158979
142094601420946015AT16GENIChomozygous791158980
142094757020947571AG17GENIChomozygous791158981
142094821820948219GA18GENIChomozygous791158982
142094838320948384GA18GENIChomozygous791158983
142094843520948436AT14GENIChomozygous791158984
142094898520948986GC23GENIChomozygous791158985
142094899820948999TA29GENIChomozygous791158986
142094900620949007AT26GENIChomozygous791158987
142094900820949009GC26GENIChomozygous791158988
142094954020949541TG23GENICpossibly homozygous791158989
142094956220949563AT24GENIChomozygous791158990
142095042120950422CA17GENIChomozygous791158991
142095107520951076CT20GENIChomozygous791158992
142095222620952227CT19GENICpossibly homozygous791158993