chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7145146563145146564TC17GENIChomozygous893244140
7145147728145147729CA13GENIChomozygous893244141
7145148101145148102AG9GENIChomozygous893244142
7145148400145148401TC13GENIChomozygous893244143
7145149929145149930GA8GENIChomozygous893244144
7145149955145149956TC17GENIChomozygous893244145
7145150310145150311CA15GENIChomozygous893244146
7145150986145150987TC13GENIChomozygous893244147
7145151089145151090GC7GENIChomozygous893244148
7145151090145151091CT8GENIChomozygous893244149
7145151136145151137TC20GENIChomozygous893244150
7145151185145151186TC16GENIChomozygous893244151
7145151315145151316GC12GENIChomozygous893244152
7145151424145151425GC18GENIChomozygous893244153
7145152087145152088GC4GENIChomozygous893244154
7145152460145152461TC16GENIChomozygous893244155
7145152860145152861GC5GENIChomozygous893244156