chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151525906151525907GT19GENIChomozygous55796886
5151526027151526028CT15GENIChomozygous55796887
5151526059151526060CT21GENIChomozygous55796888
5151526108151526109CT23GENIChomozygous56129158
5151526224151526225AG21GENIChomozygous55796889
5151526430151526432CA--29GENIChomozygous55796890
5151526587151526588CA32GENIChomozygous55796891
5151526927151526928GC37GENIChomozygous55796892
5151527070151527071CT19GENIChomozygous55796893
5151527248151527249GA8GENIChomozygous55796894
5151527609151527610CCTTTTTTTTTT1GENIChomozygous56494902
5151527791151527792CT9GENIChomozygous55796899
5151527996151527997GA16GENIChomozygous55796900
5151528016151528017CCTT8GENIChomozygous55796901
5151528037151528038CCTTTTT4GENICheterozygous55796904
5151528037151528038CCTTTTTTTTTT4GENICheterozygous56494903
5151528329151528330GA21GENIChomozygous55796906
5151529316151529332TCAATCAATCAACCAA----------------8GENIChomozygous55796907
5151530452151530453TC31GENIChomozygous55796909
5151531032151531033GA18GENIChomozygous55796910
5151531071151531072TTAA15GENIChomozygous55796911
5151532097151532098AAT11GENIChomozygous55796912
5151532349151532350GA22GENIChomozygous55796913
5151532466151532467AT9GENIChomozygous55796914