chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
147983062679830627GA79GENICpossibly homozygous142445171
147983231379832349CCTCAGCTGGTGACTTGGCCTCCACTGGAGATTTGA31GENICheterozygous144106740
147983331279833313GA47GENIChomozygous142445172
147983593879835939TG66GENICpossibly homozygous142445173
147983764379837644AG46GENIChomozygous142445174
147983850079838501CT53GENIChomozygous142445175
147983861079838611CT53GENIChomozygous142445176
147983873779838738AG46GENIChomozygous142445177
147983876179838762CT46GENIChomozygous142445178
147983970879839709CT33GENIChomozygous142445179
147983233679832337A31GENICheterozygous403363734
147983233679832337AG31GENICheterozygous154863529
147983252979832529CCTCAGCTGGGGACTTGGCCTCAGCTGGTGACTTGG18GENIChomozygous142422057