chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
136883253268832533CA10GENIChomozygous983260088
136883457768834578GA16GENIChomozygous983260089
136883481168834812AG27GENIChomozygous983260090
136883842068838421TC20GENIChomozygous983260091
136883977268839773GT5GENIChomozygous983260092
136884333568843336GA8GENIChomozygous983260093
136884527668845277AT23GENIChomozygous983260094
136884536968845370CT11GENIChomozygous983260095
136884649868846499GC27GENIChomozygous983260096
136884667168846672GA18GENIChomozygous983260097
136884683568846836CT21GENICpossibly homozygous983260098
136885024968850250AT15GENIChomozygous983260099
136885036868850369TA11GENIChomozygous983260100
136885083968850840TC21GENIChomozygous983260101
136885168968851690AG28GENICpossibly homozygous983260102
136885255868852559AC6GENIChomozygous983260103
136885300468853005TC10GENIChomozygous983260104
136885318368853184CT20GENIChomozygous983260105
136885352068853521AG20GENIChomozygous983260106
136885416168854162GA17GENIChomozygous983260107
136885515068855151CT19GENIChomozygous983260108
136885528768855288CT23GENIChomozygous983260109
136885646368856464AG12GENIChomozygous983260110
136885664968856650TC21GENIChomozygous983260111
136885681268856813AG19GENIChomozygous983260112
136885927868859279AG16GENIChomozygous983260113
136885936868859369AG9GENIChomozygous983260114
136885941568859416AG9GENIChomozygous983260115