chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115486701115486702AG25GENIChomozygous112815742
4115489218115489219GA30GENIChomozygous112815744
4115489382115489383GA13GENIChomozygous112815746
4115489482115489483TC13GENIChomozygous112815748
4115491995115491996TC22GENIChomozygous112815750
4115492032115492033CT23GENIChomozygous112815752
4115492076115492077CA24GENIChomozygous112815754
4115492226115492227GA42GENIChomozygous112815756
4115493939115493940CT19GENIChomozygous112815758
4115494085115494086TC47GENIChomozygous112815760
4115494950115494951CT18GENIChomozygous112815762
4115495126115495127TC28GENIChomozygous112815764
4115496389115496390GT18GENIChomozygous112815766
4115497184115497185AC33GENIChomozygous112815768
4115498628115498629CT28GENIChomozygous112815772
4115500945115500946GA14GENIChomozygous112815774
4115501626115501627TC18GENIChomozygous112815780
4115502064115502065TC25GENIChomozygous112815782
4115502552115502553GA26GENIChomozygous112815784
4115503033115503034AC14GENIChomozygous112815786
4115503344115503345GA23GENIChomozygous112815788
4115503762115503763AC14GENIChomozygous119570369
4115504967115504968AG21GENIChomozygous112815796
4115506118115506119CA25GENIChomozygous112815798
4115506437115506438TC30GENIChomozygous112815800
4115507188115507189GC17GENIChomozygous112815802
4115509055115509056TC22GENIChomozygous112815804
4115511475115511476AG20GENIChomozygous112815808
4115514850115514851TC24GENIChomozygous112815812
4115514913115514914AT21GENIChomozygous113047988
4115514914115514915TA20GENIChomozygous113047990