chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142093570320935704CT7GENIChomozygous989091052
142093596520935966GA13GENIChomozygous989091053
142093635020936351GA20GENIChomozygous989091054
142093903820939039AT13GENIChomozygous989091055
142093939420939395AG36GENIChomozygous989091056
142094222920942230TC26GENIChomozygous989091057
142094223220942233CA28GENIChomozygous989091058
142094261420942615GC24GENIChomozygous989091059
142094468420944685AG16GENIChomozygous989091060
142094491220944913AG18GENIChomozygous989091061
142094601420946015AT16GENIChomozygous989091062
142094757020947571AG19GENIChomozygous989091063
142094821820948219GA7GENIChomozygous989091064
142094838320948384GA26GENIChomozygous989091065
142094843520948436AT26GENIChomozygous989091066
142094898520948986GC35GENIChomozygous989091067
142094898920948990TA35GENIChomozygous989091068
142094899220948993GT35GENIChomozygous989091069
142094899820948999TA35GENIChomozygous989091070
142094900620949007AT33GENIChomozygous989091071
142094900820949009GC33GENIChomozygous989091072
142094954020949541TG20GENIChomozygous989091073
142094956220949563AT16GENIChomozygous989091074
142095042120950422CA26GENIChomozygous989091075
142095107520951076CT21GENIChomozygous989091076
142095222620952227CT31GENIChomozygous989091077