chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151525906151525907GT14GENIChomozygous634382965
5151526027151526028CT14GENIChomozygous634382966
5151526059151526060CT11GENIChomozygous634382967
5151526224151526225AG14GENIChomozygous634382968
5151526430151526432CA--28GENIChomozygous747391634
5151526587151526588CA24GENIChomozygous634382969
5151526927151526928GC44GENIChomozygous634382970
5151527070151527071CT33GENIChomozygous634382971
5151527248151527249GA33GENICpossibly homozygous634382972
5151527609151527610CCTTTTTTTTTT2GENIChomozygous747391636
5151527704151527705A-2GENIChomozygous747391637
5151527791151527792CT20GENIChomozygous634382973
5151527996151527997GA19GENIChomozygous634382974
5151528016151528017CCTT15GENIChomozygous747391638
5151528037151528038CCTTTTT10GENICheterozygous747391641
5151528037151528038CCTTTTTTTTTT10GENICheterozygous747391642
5151528329151528330GA18GENIChomozygous634382975
5151529316151529332TCAATCAATCAACCAA----------------11GENIChomozygous747391643
5151530452151530453TC29GENIChomozygous634382976
5151531032151531033GA34GENIChomozygous634382977
5151531071151531072TTAA24GENIChomozygous747391645
5151532097151532098AAT11GENIChomozygous747391646
5151532349151532350GA17GENIChomozygous634382978
5151532466151532467AT15GENIChomozygous634382979