chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
58250390982503910TA104GENIChomozygous506438727
58250400682504007A-78GENIChomozygous685661069
58250413182504132CT95GENIChomozygous506438728
58250456482504565AAG32GENIChomozygous685661070
58250464182504642GGA26GENIChomozygous685661071
58250527982505280CCT19GENICpossibly homozygous685661072
58250572982505730TTCC19GENICheterozygous685661073
58250573182505732TC22GENICheterozygous506438729
58250595582505956CT51GENIChomozygous506438730
58250602582506026CT55GENIChomozygous506438731
58250663782506638TC59GENIChomozygous506438732
58250776582507766TC60GENIChomozygous506438733
58250807382508074AC24GENIChomozygous508696070
58250807882508084CTCTCT------19GENIChomozygous685661074
58250860582508607TC--17GENIChomozygous685661075
58250862382508624CCTGTG30GENIChomozygous685661076
58250875182508757GTGTGT------9GENICpossibly homozygous685661077
58250887282508873GA60GENIChomozygous508696071
58250895182508952TTTG62GENIChomozygous685661079
58250897982508980TC73GENICpossibly homozygous506438734
58250924782509248TC42GENIChomozygous506438735
58250942982509430GT51GENIChomozygous506438736
58250947382509474CA48GENIChomozygous506438737
58250993882509939C-23GENICpossibly homozygous685661080