chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141714512317145124AG51GENIChomozygous48547698
141714523417145235CT23GENIChomozygous48547699
141714523717145238CT22GENIChomozygous48547700
141714543617145437AT34GENIChomozygous48547701
141714643117146432GGTT19GENICpossibly homozygous48547702
141714643117146432GGTTT19GENICheterozygous48956514
141714688117146882TC17GENIChomozygous48547703
141714729217147293TA17GENIChomozygous48547704
141714759417147595TC44GENICpossibly homozygous48547705
141714775117147752TG33GENIChomozygous48547706
141714793917147940CCAT1GENIChomozygous49324047
141714893517148936CT37GENICpossibly homozygous48547710
141714897817148979TG38GENIChomozygous48547711
141714907817149079GA27GENIChomozygous48547712
141714929817149299TC42GENIChomozygous48547713
141714930717149308CT43GENIChomozygous48547714
141715017517150176GA29GENIChomozygous48547715