chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
860168306016831TC20GENIChomozygous116426193
860184766018477AC16GENIChomozygous116426194
860186496018650TG27GENIChomozygous116426195
860198226019823GC41GENIChomozygous116426196
860200296020030TC30GENIChomozygous116426197
860217646021765GA29GENIChomozygous116426198
860228046022805AG31GENICpossibly homozygous116426199
860235376023538TC15GENIChomozygous116426200
860243316024332CT27GENIChomozygous116426201
860309396030940CT3GENIChomozygous116426202
860310306031031CT16GENIChomozygous116426203
860312026031203TC13GENIChomozygous116426204
860320096032010GA21GENIChomozygous116426205
860332086033209CA26GENICpossibly homozygous116426206
860342506034251GA23GENIChomozygous116426208