chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141714512317145124AG27GENIChomozygous48547698
141714523417145235CT17GENIChomozygous48547699
141714523717145238CT18GENIChomozygous48547700
141714543617145437AT26GENIChomozygous48547701
141714643117146432GGTT12GENICheterozygous48547702
141714643117146432GGTTT12GENICheterozygous48956514
141714688117146882TC10GENIChomozygous48547703
141714729217147293TA21GENIChomozygous48547704
141714759417147595TC19GENIChomozygous48547705
141714775117147752TG20GENIChomozygous48547706
141714793917147940CCAT4GENIChomozygous49324047
141714893517148936CT24GENIChomozygous48547710
141714897817148979TG14GENIChomozygous48547711
141714907817149079GA15GENIChomozygous48547712
141714929817149299TC27GENIChomozygous48547713
141714930717149308CT29GENIChomozygous48547714
141715017517150176GA16GENIChomozygous48547715
141714643117146432GGT12GENICheterozygous49277942