chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141714512317145124AG23GENIChomozygous48547698
141714523417145235CT20GENIChomozygous48547699
141714523717145238CT18GENIChomozygous48547700
141714543617145437AT20GENIChomozygous48547701
141714643117146432GGTT22GENIChomozygous48547702
141714688117146882TC19GENIChomozygous48547703
141714729217147293TA23GENIChomozygous48547704
141714759417147595TC19GENIChomozygous48547705
141714775117147752TG25GENICpossibly homozygous48547706
141714794517147947TG--6GENIChomozygous48547707
141714796117147963TA--4GENIChomozygous48956518
141714860317148604AAG7GENICheterozygous48547708
141714860317148604AAAG7GENICpossibly homozygous48547709
141714893517148936CT22GENIChomozygous48547710
141714897817148979TG20GENIChomozygous48547711
141714907817149079GA32GENIChomozygous48547712
141714929817149299TC32GENIChomozygous48547713
141714930717149308CT34GENIChomozygous48547714
141715017517150176GA22GENIChomozygous48547715