chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151525906151525907GT18GENIChomozygous517661675
5151526027151526028CT26GENIChomozygous517661676
5151526059151526060CT26GENIChomozygous517661677
5151526108151526109CT29GENIChomozygous517661678
5151526224151526225AG24GENIChomozygous517661679
5151526430151526432CA--25GENIChomozygous689114795
5151526587151526588CA32GENIChomozygous517661680
5151526927151526928GC31GENIChomozygous517661681
5151527070151527071CT42GENIChomozygous517661682
5151527248151527249GA34GENIChomozygous517661683
5151527627151527628T-3GENICheterozygous689114796
5151527664151527665TC8GENICpossibly homozygous517661684
5151527704151527705A-6GENIChomozygous689114797
5151527705151527706AG12GENICheterozygous517661685
5151527791151527792CT27GENIChomozygous517661686
5151527996151527997GA20GENIChomozygous517661687
5151528016151528017CCTT16GENIChomozygous689114798
5151528037151528038C-15GENICheterozygous689114799
5151528037151528038CCTTTTT14GENIChomozygous689114801
5151528049151528050GT19GENICheterozygous517661688
5151528329151528330GA19GENIChomozygous517661689
5151529316151529332TCAATCAATCAACCAA----------------6GENIChomozygous689114802
5151529328151529329CCCAAT6GENICheterozygous689114803
5151530452151530453TC34GENIChomozygous517661690
5151531032151531033GA25GENIChomozygous517661691
5151531071151531072TTAA16GENIChomozygous689114804
5151532097151532098AAT9GENIChomozygous689114805
5151532349151532350GA18GENIChomozygous517661692
5151532466151532467AT9GENIChomozygous517661693