chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3180989541180989542CT14GENIChomozygous59648612
3180996242180996243T-32GENIChomozygous57821196
3180996244180996245GGCAGC34GENIChomozygous57821198
3181006580181006602AGAGAGAGAGAGAGAGAGAGAG----------------------6GENICheterozygous59648614
3181014945181014946TC25GENIChomozygous57821262
3181018911181018912TTG7GENICpossibly homozygous58635153
3181020402181020405GAG---9GENIChomozygous57821270
3181020767181020768GA29GENIChomozygous59648616
3181027690181027691GGT20GENIChomozygous59648618
3181036974181036975A-27GENIChomozygous59648620
3181044963181044964CCCTCCT8GENIChomozygous58635158
3180990618180990619GGATA14GENICpossibly homozygous59109391
3181015655181015656T-14GENICheterozygous58858263