chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3107372857107372858TC28GENIChomozygous72074338
3107374964107374965TC29GENIChomozygous72074344
3107381199107381200CT16GENICpossibly homozygous72074352
3107382345107382346GT10GENIChomozygous72074364
3107384188107384189TC28INTERGENIChomozygous72074386
3107393170107393171GA34INTERGENIChomozygous73628485
3107390957107390958GA24INTERGENICpossibly homozygous74860243
3107401793107401794GA7INTERGENIChomozygous73750964
3107402129107402130AG25GENIChomozygous72074442
3107411162107411163GA27GENIChomozygous74860246
3107411181107411182GA28GENIChomozygous72074462
3107415483107415484AG32GENIChomozygous72074478
3107416120107416121CA12GENIChomozygous72074484