chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154455069044550691AG7GENIChomozygous112879311
154455866644558667GC8GENIChomozygous113079243
154455867444558675G10GENIChomozygous129251617
154455868144558682C12GENIChomozygous129251618
154455868644558687T13GENIChomozygous129251619
154455871444558715T20GENIChomozygous129251620
154455871744558718G19GENIChomozygous129251621
154455873044558731T18GENIChomozygous129251622
154455874044558742GA18GENIChomozygous129251623
154455874944558749T18GENIChomozygous129251624
154455875244558753G17GENIChomozygous129251625
154455879244558793C19GENIChomozygous129251626
154455879944558799C19GENIChomozygous129251627
154455880544558808GCC15GENIChomozygous129251628
154455881644558821CCCAT16GENICpossibly homozygous129251629
154455882444558824C15GENIChomozygous129251630
154456546344565466GTG12GENIChomozygous129251632
154456547944565481GC10GENIChomozygous129251633
154456548244565482G10GENIChomozygous129251634
154456549144565492C10GENIChomozygous129251635
154456549844565499G9GENIChomozygous129251636
154456550744565507T8GENIChomozygous129251637
154456551544565516G6GENIChomozygous129251638
154456552244565523G5GENIChomozygous129251639
154456552444565525GC5GENIChomozygous124070719
154456553744565538GC4GENIChomozygous124070720
154456554944565553AAGC3GENIChomozygous129251640
154456555644565556T2GENIChomozygous129251641
154456557044565571G1GENIChomozygous129251642
154460265244602653T19GENICheterozygous129251665
154460869844608698A24GENIChomozygous129251669
154461575944615761TC19GENICheterozygous130149263