chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109121237891212379TTGC5GENIChomozygous51539277
109121364691213647GA21GENIChomozygous51929147
109121530891215330TCCCGCCTCTACTCTGCCCCCC----------------------7GENIChomozygous51929150
109121580591215806GGC4GENICheterozygous51929153
109121584891215858GTGTGTGTGT----------4GENICheterozygous51539281
109121636091216361GA24GENIChomozygous51539282
109121671291216713CT26GENIChomozygous51539283
109121793791217938C-24GENIChomozygous51739178
109121960391219604TC22GENIChomozygous51929156
109121968791219688GT16GENIChomozygous51539284
109122108491221085GA21GENIChomozygous51539288
109122121991221223TTTT----9GENIChomozygous51539290
109122138991221390TG20GENICheterozygous51539292
109122147791221478CG15GENICpossibly homozygous51539293
109122163491221635AG26GENIChomozygous51539295
109122213291222133GA20GENICpossibly homozygous51539296