chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104672066546720666GC17GENIChomozygous116586554
104672390246723903AC19GENIChomozygous116877904
104672715646727157TC30GENIChomozygous116877908
104672882946728830AG11GENIChomozygous116586556
104672919146729192GA20GENIChomozygous116877910
104672992046729921GA21GENIChomozygous117078155
104673474046734741GA28GENIChomozygous116877912
104673903546739036AG20GENIChomozygous116877914
104674335946743360CA30GENIChomozygous116586560
104674470546744706AG33GENIChomozygous116586564
104674513246745133GA39GENIChomozygous116877916
104674915346749154AG24GENIChomozygous116586572
104675068646750687TC22GENIChomozygous116586574
104675126846751269TC50GENIChomozygous116877918
104675171146751712GA34GENIChomozygous116877920
104675266746752668GT23GENIChomozygous116877922
104675342346753424CT30GENIChomozygous116877924
104675347746753478AG17GENIChomozygous116772954
104675368346753684GC19GENIChomozygous116877926
104675409846754099TC22GENIChomozygous116586578
104675409946754100GA22GENIChomozygous116877928
104675449146754492GA20GENIChomozygous116877930
104675541546755416CA13GENIChomozygous116877932
104675615746756158AG22GENIChomozygous116586580
104675755046757551AG25GENIChomozygous116586582
104675904946759050GA28GENIChomozygous116877934
104676144746761448TC34GENIChomozygous116586592
104676215546762156CT29GENIChomozygous116877936