chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37246157872461579GA7GENIChomozygous111608085
37246185872461859CT14GENIChomozygous111608086
37246287572462876GT6GENIChomozygous111608088
37246314672463147AG15GENIChomozygous119675448
37246333772463338CT12GENIChomozygous111923316
37246344172463442AT18GENIChomozygous111608091
37246424172464242TG11GENIChomozygous111608093
37246445372464454AC5GENIChomozygous111608094
37246647872466479AG13GENIChomozygous111608103
37246666972466670AG10GENIChomozygous111608105
37246713772467138GA12GENIChomozygous119675449
37246714472467145TG11GENIChomozygous111608107
37246779372467794AG12GENICpossibly homozygous119675450
37246784772467848TA10GENICpossibly homozygous111608108
37246888572468886CA10GENIChomozygous119675451
37246938372469384TC7GENIChomozygous111608112
37247021372470214AC8GENIChomozygous119675452
37247122172471222CA5GENIChomozygous111608115
37247123572471236GA5GENIChomozygous119675453
37247156272471563CT6GENIChomozygous119675454
37247198072471981TA4GENIChomozygous111608117
37247202272472023CT5GENIChomozygous119675455
37247592172475922CT8GENIChomozygous111608126
37247699072476991CT8GENIChomozygous111608128
37247883272478833CT9GENIChomozygous111608129
37247961872479619TC14GENIChomozygous111608130
37247964672479647CG13GENIChomozygous111608131
37247966072479661GA9GENIChomozygous111608132
37248103272481033AG11GENIChomozygous111608134
37248180772481808AC12GENIChomozygous111608135