chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115486074115486075AG21GENIChomozygous112815740
4115486701115486702AG15GENIChomozygous112815742
4115489218115489219GA22GENIChomozygous112815744
4115489382115489383GA30GENIChomozygous112815746
4115491995115491996TC29GENIChomozygous112815750
4115492032115492033CT27GENIChomozygous112815752
4115492076115492077CA30GENIChomozygous112815754
4115492226115492227GA19GENIChomozygous112815756
4115493939115493940CT29GENIChomozygous112815758
4115494085115494086TC15GENIChomozygous112815760
4115494950115494951CT34GENIChomozygous112815762
4115495126115495127TC20GENIChomozygous112815764
4115496389115496390GT13GENIChomozygous112815766
4115497184115497185AC19GENIChomozygous112815768
4115498485115498486AC28GENIChomozygous112815770
4115498628115498629CT23GENIChomozygous112815772
4115500945115500946GA3GENIChomozygous112815774
4115501132115501133TC9GENIChomozygous112815776
4115501160115501161AG8GENIChomozygous112815778
4115501626115501627TC17GENIChomozygous112815780
4115502064115502065TC15GENIChomozygous112815782
4115502552115502553GA15GENIChomozygous112815784
4115503600115503601TG6GENIChomozygous112815790
4115504967115504968AG22GENIChomozygous112815796
4115506118115506119CA26GENIChomozygous112815798
4115506437115506438TC10GENIChomozygous112815800
4115507188115507189GC17GENIChomozygous112815802
4115509055115509056TC19GENIChomozygous112815804
4115511131115511132TA19GENIChomozygous112815806
4115511475115511476AG25GENIChomozygous112815808
4115514850115514851TC31GENIChomozygous112815812
4115514913115514914AT25GENIChomozygous113047988
4115514914115514915TA24GENIChomozygous113047990