chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142093570320935704CT19GENIChomozygous976962809
142093596520935966GA21GENIChomozygous976962810
142093635020936351GA16GENIChomozygous976962811
142093903820939039AT28GENIChomozygous976962812
142093939420939395AG28GENIChomozygous976962813
142094222920942230TC19GENIChomozygous976962814
142094223220942233CA18GENIChomozygous976962815
142094261420942615GC20GENIChomozygous976962816
142094468420944685AG34GENIChomozygous976962817
142094601420946015AT26GENIChomozygous976962818
142094757020947571AG20GENIChomozygous976962819
142094821820948219GA23GENIChomozygous976962820
142094838320948384GA15GENIChomozygous976962821
142094843520948436AT22GENIChomozygous976962822
142094898520948986GC19GENIChomozygous976962823
142094898920948990TA18GENIChomozygous976962824
142094899220948993GT18GENIChomozygous976962825
142094899820948999TA16GENIChomozygous976962826
142094900620949007AT18GENIChomozygous976962827
142094900820949009GC18GENIChomozygous976962828
142094954020949541TG17GENICpossibly homozygous976962829
142094956220949563AT23GENIChomozygous976962830
142095042120950422CA20GENIChomozygous976962831
142095107520951076CT36GENIChomozygous976962832
142095222620952227CT13GENIChomozygous976962833