chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
147983062679830627GA21GENIChomozygous142445171
147983231379832349CCTCAGCTGGTGACTTGGCCTCCACTGGAGATTTGA13GENICpossibly homozygous144106740
147983331279833313GA19GENIChomozygous142445172
147983593879835939TG15GENIChomozygous142445173
147983233679832337A13GENICpossibly homozygous403363734
147983233679832337AG13GENICheterozygous154863529
147983764379837644AG20GENIChomozygous142445174
147983850079838501CT17GENIChomozygous142445175
147983861079838611CT21GENIChomozygous142445176
147983873779838738AG24GENIChomozygous142445177
147983876179838762CT23GENIChomozygous142445178
147983970879839709CT18GENIChomozygous142445179
147983252979832529CCTCAGCTGGGGACTTGGCCTCAGCTGGTGACTTGG5GENIChomozygous142422057