chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6144513775144513776AG5GENIChomozygous625239436
6144513777144513778AG5GENIChomozygous625239437
6144515224144515225GA12GENICheterozygous625239438
6144516170144516171AG12GENICheterozygous625239439
6144516656144516657CT16GENIChomozygous625239440
6144517233144517234CT8GENICheterozygous625239441
6144518272144518273AT25GENICpossibly homozygous625239442
6144518417144518418CCG10GENIChomozygous740750710
6144518607144518608GT21GENICpossibly homozygous625239443
6144518730144518731GA8GENIChomozygous625239444
6144518869144518870CA3GENIChomozygous625239445
6144520045144520046AT9GENIChomozygous625239446
6144520151144520152TC13GENICpossibly homozygous625239447
6144520883144520884CCA4GENIChomozygous740750711
6144520887144520888CCT3GENIChomozygous740750712
6144521069144521070GC8GENICpossibly homozygous625239448
6144521666144521667GA12GENICpossibly homozygous625239449
6144523383144523384TC3GENIChomozygous625239450
6144523436144523437AG6GENIChomozygous625239451
6144523524144523525CT13GENICheterozygous625239452
6144523689144523690C-17GENIChomozygous740750713
6144523819144523820CT19GENIChomozygous625239453
6144524668144524669AG1GENIChomozygous625239454