chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151525906151525907GT24GENIChomozygous513240156
5151526027151526028CT20GENIChomozygous513240157
5151526059151526060CT16GENIChomozygous513240158
5151526224151526225AG25GENIChomozygous513240159
5151526430151526432CA--28GENIChomozygous687462975
5151526587151526588CA24GENICpossibly homozygous513240160
5151526927151526928GC24GENIChomozygous513240161
5151527070151527071CT18GENIChomozygous513240162
5151527248151527249GA23GENIChomozygous513240163
5151527627151527628T-5GENIChomozygous687462976
5151527664151527665TC11GENIChomozygous513240164
5151527704151527705A-5GENIChomozygous687462977
5151527705151527706AG10GENICheterozygous513240165
5151527791151527792CT14GENIChomozygous513240166
5151527996151527997GA21GENIChomozygous513240167
5151528016151528017CCTT17GENIChomozygous687462978
5151528037151528038CT27GENICheterozygous513240168
5151528037151528038C-23GENICheterozygous687462979
5151528037151528038CCTTTTT20GENIChomozygous687462981
5151528329151528330GA18GENIChomozygous513240169
5151529316151529332TCAATCAATCAACCAA----------------8GENIChomozygous687462982
5151530452151530453TC27GENIChomozygous513240170
5151531032151531033GA25GENIChomozygous513240171
5151531071151531072TTAA17GENIChomozygous687462983
5151532097151532098AAT13GENIChomozygous687462984
5151532349151532350GA35GENIChomozygous513240172
5151532466151532467AT29GENIChomozygous513240173