chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1178526948178526949CT26INTERGENIChomozygous810666812
1178527101178527102AG11INTERGENIChomozygous810666813
1178527840178527841TC26INTERGENIChomozygous810666814
1178528043178528044TA15INTERGENIChomozygous810666815
1178529240178529241CA10INTERGENICpossibly homozygous810666816
1178529589178529590GA18INTERGENIChomozygous810666817
1178530100178530101GT25INTERGENIChomozygous810666818
1178530884178530885AT41INTERGENIChomozygous810666819
1178531607178531608GA29INTERGENICpossibly homozygous810666820
1178531673178531674AT22INTERGENIChomozygous810666821