chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151525906151525907GT29GENIChomozygous55796886
5151526027151526028CT35GENIChomozygous55796887
5151526059151526060CT39GENIChomozygous55796888
5151526224151526225AG28GENIChomozygous55796889
5151526430151526432CA--32GENIChomozygous55796890
5151526587151526588CA51GENIChomozygous55796891
5151526927151526928GC41GENIChomozygous55796892
5151527070151527071CT46GENIChomozygous55796893
5151527248151527249GA35GENIChomozygous55796894
5151527627151527628T-14GENICheterozygous55796895
5151527664151527665TC12GENIChomozygous55796896
5151527704151527705A-6GENIChomozygous55796897
5151527705151527706AG10GENICheterozygous55796898
5151527791151527792CT20GENIChomozygous55796899
5151527996151527997GA26GENIChomozygous55796900
5151528016151528017CCTT15GENIChomozygous55796901
5151528037151528038CT24GENICheterozygous55796902
5151528037151528038C-23GENICheterozygous55796903
5151528037151528038CCTTTTT20GENIChomozygous55796904
5151528329151528330GA27GENIChomozygous55796906
5151529316151529332TCAATCAATCAACCAA----------------6GENIChomozygous55796907
5151529328151529329CCCAAT10GENICheterozygous55796908
5151530452151530453TC34GENIChomozygous55796909
5151531032151531033GA26GENIChomozygous55796910
5151531071151531072TTAA18GENIChomozygous55796911
5151532097151532098AAT24GENIChomozygous55796912
5151532349151532350GA46GENIChomozygous55796913
5151532466151532467AT20GENIChomozygous55796914