chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
58250390982503910TA21GENIChomozygous667140653
58250400682504007A-18GENIChomozygous767415122
58250413182504132CT25GENIChomozygous667140654
58250456482504565AAG11GENIChomozygous767415123
58250464182504642GGA11GENICpossibly homozygous767415124
58250526082505261TC12GENIChomozygous667140655
58250527982505280CCT5GENICheterozygous767415125
58250527982505280CCTT5GENICheterozygous767415126
58250572982505730TTCC1GENIChomozygous767415127
58250602582506026CT24GENIChomozygous667140656
58250644082506441CCA7GENICheterozygous767415129
58250644182506442A-7GENICheterozygous767415128
58250663782506638TC20GENIChomozygous667140657
58250776582507766TC22GENIChomozygous667140658
58250807382508074AC16GENIChomozygous667140659
58250807882508084CTCTCT------15GENIChomozygous767415130
58250860582508607TC--27GENIChomozygous767415131
58250862382508624CCTGTG31GENIChomozygous767415132
58250875182508767GTGTGTGTGTGTGTGT----------------13GENIChomozygous767415133
58250895182508952TTTG27GENIChomozygous767415137
58250913982509140T-26GENIChomozygous767415139
58250924782509248TC23GENIChomozygous667140660
58250939982509400CT22GENIChomozygous667140661
58250942982509430GT20GENIChomozygous667140662
58250947382509474CA15GENIChomozygous667140663
58250993882509939C-6GENICheterozygous767415140