chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141714512317145124AG10GENIChomozygous48547698
141714523417145235CT2GENIChomozygous48547699
141714523717145238CT1GENIChomozygous48547700
141714543617145437AT3GENIChomozygous48547701
141714643117146432GGTT2GENICheterozygous48547702
141714643117146432GGT2GENICheterozygous49277942
141714688117146882TC7GENIChomozygous48547703
141714729217147293TA10GENICpossibly homozygous48547704
141714759417147595TC9GENICpossibly homozygous48547705
141714775117147752TG8GENICpossibly homozygous48547706
141714893517148936CT9GENICpossibly homozygous48547710
141714897817148979TG6GENIChomozygous48547711
141714907817149079GA19GENIChomozygous48547712
141714929817149299TC5GENIChomozygous48547713
141714930717149308CT6GENIChomozygous48547714
141715017517150176GA15GENIChomozygous48547715