chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3148234690148234691TC47GENIChomozygous111769076
3148234991148234992CT41GENIChomozygous111769078
3148238151148238152CT46GENIChomozygous111769080
3148239106148239107GA79GENICpossibly homozygous111769082
3148239828148239829TG54GENIChomozygous111769084
3148240119148240120CT46GENIChomozygous111769086
3148240197148240198TA60GENICpossibly homozygous111769088
3148240200148240201TA62GENIChomozygous111769090
3148240878148240879GA61GENIChomozygous111769092
3148241050148241051TC46GENICpossibly homozygous111769094
3148241501148241502GA66GENIChomozygous111769096
3148242127148242128GA65GENIChomozygous111769098
3148243472148243473CT55GENIChomozygous111769100
3148244495148244496AT57GENIChomozygous111769102
3148244506148244507CG59GENIChomozygous111769104