chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1222478664222478665CT11GENIChomozygous108546750
1222479820222479821CG18GENICpossibly homozygous109449748
1222480160222480161GA26GENIChomozygous109449749
1222481309222481310TA16GENIChomozygous108546754
1222481511222481512CT22GENIChomozygous109449750
1222481793222481794TG18GENIChomozygous109449751
1222482552222482553AG20GENIChomozygous108546756
1222485774222485775GA30GENIChomozygous109449752
1222488439222488440AC32GENIChomozygous109449753
1222488483222488484GA36GENIChomozygous109449754
1222488662222488663CG29GENIChomozygous108546769
1222489229222489230TA28GENIChomozygous109449755
1222489986222489987GA22GENIChomozygous109449756
1222490410222490411TC22GENIChomozygous109449757
1222491884222491885GA29GENIChomozygous109449758
1222493800222493801TC18GENIChomozygous108995538
1222494944222494945AG26GENIChomozygous108995539