chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1163444193163444194CT60GENIChomozygous108348144
1163444537163444538GT35GENIChomozygous108348146
1163445384163445385GC37GENICpossibly homozygous108348148
1163445586163445587GC18GENICpossibly homozygous108952498
1163445843163445844GA61GENIChomozygous108348150
1163445887163445888GA56GENICpossibly homozygous108952499
1163448308163448309AC38GENIChomozygous108348156
1163449285163449286AG56GENIChomozygous108348158
1163453410163453411AC53GENICpossibly homozygous108348180
1163456135163456136AG32GENIChomozygous108348182