chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151525906151525907GT9GENIChomozygous557938196
5151526027151526028CT18GENIChomozygous557938197
5151526059151526060CT18GENIChomozygous557938198
5151526108151526109CT17GENIChomozygous557938199
5151526224151526225AG26GENIChomozygous557938200
5151526430151526432CA--25GENIChomozygous705041095
5151526587151526588CA31GENICpossibly homozygous557938201
5151526927151526928GC24GENIChomozygous557938202
5151527070151527071CT11GENIChomozygous557938203
5151527248151527249GA18GENIChomozygous557938204
5151527609151527610CCTTTTTTTTTT4GENIChomozygous705041097
5151527627151527628T-2GENIChomozygous705041098
5151527704151527705A-4GENICheterozygous705041099
5151527791151527792CT15GENIChomozygous557938205
5151527996151527997GA16GENIChomozygous557938206
5151528016151528017CCTT11GENIChomozygous705041100
5151528037151528038CCTT6GENICheterozygous705041102
5151528037151528038CCTTTTTTTTTT6GENICheterozygous705041104
5151528329151528330GA16GENIChomozygous557938207
5151529316151529332TCAATCAATCAACCAA----------------8GENIChomozygous705041105
5151530452151530453TC24GENIChomozygous557938208
5151531032151531033GA15GENIChomozygous557938209
5151531071151531072TTAA13GENIChomozygous705041107
5151532097151532098AAT7GENIChomozygous705041108
5151532349151532350GA18GENIChomozygous557938210
5151532466151532467AT15GENIChomozygous557938211