chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1244921307244921308TC35GENIChomozygous135854273
1244921932244921933CT31GENICpossibly homozygous135854274
1244922686244922688TT20GENIChomozygous135470601
1244922710244922711AG26GENIChomozygous135854275
1244922916244922917CT20GENIChomozygous135854276
1244923181244923181C9GENIChomozygous135470602
1244924098244924099TA21GENIChomozygous135854277
1244924099244924100CG21GENIChomozygous135854278
1244924752244924753GA29GENIChomozygous135854279
1244925332244925333TA25GENIChomozygous135854280
1244928815244928816GA16GENIChomozygous135854281
1244928939244928940AG14GENIChomozygous135854282
1244931743244931744G20GENIChomozygous135470603