chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109121237991212381GC--8GENIChomozygous52809339
109121286691212867CA14GENIChomozygous51539279
109121580691215807C-15GENICheterozygous51539280
109121585291215858GTGTGT------8GENICheterozygous52809342
109121636091216361GA31GENIChomozygous51539282
109121671291216713CT44GENIChomozygous51539283
109121968791219688GT50GENIChomozygous51539284
109121979491219795CG48GENIChomozygous51539285
109122068291220683GA35GENIChomozygous51539286
109122075391220754AT45GENIChomozygous51539287
109122108491221085GA21GENIChomozygous51539288
109122121891221226CTTTTTTT--------19GENICpossibly homozygous51539289
109122121891221225CTTTTTT-------19GENICheterozygous52508755
109122126391221264CG24GENIChomozygous51539291
109122147791221478CG40GENIChomozygous51539293
109122158091221581CT26GENIChomozygous51539294
109122163491221635AG32GENIChomozygous51539295
109122213291222133GA30GENIChomozygous51539296