chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1173533902173533903TG22GENIChomozygous108961205
1173534575173534576TG30GENIChomozygous108389132
1173534654173534655CG35GENIChomozygous108961206
1173534798173534799CA30GENIChomozygous108389134
1173534855173534856CA24GENIChomozygous108389136
1173535134173535135AC29GENIChomozygous108961207
1173535272173535273TA31GENIChomozygous108389138
1173535292173535293GA38GENIChomozygous108389140
1173535418173535419GA45GENICpossibly homozygous108961208
1173535899173535900AG17GENIChomozygous108389144
1173536176173536177GA27GENIChomozygous108389146
1173538013173538014GA18GENIChomozygous108961209
1173539496173539497CA26GENIChomozygous108961210
1173540248173540249GA23GENIChomozygous108961211
1173540826173540827AG25GENIChomozygous108961212
1173541458173541459CT14GENIChomozygous108389152