chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3110877018110877019AG19GENIChomozygous111673557
3110879489110879490TA16GENIChomozygous112292520
3110879499110879499T17GENIChomozygous130907869
3110881877110881880TTG8GENIChomozygous130907870
3110886529110886530TC5GENIChomozygous112292524
3110891813110891813A18GENICheterozygous130907871
3110892202110892202AAAC17GENICpossibly homozygous130907872
3110894832110894833AG19GENIChomozygous111673565
3110895728110895729CT17GENIChomozygous112292526
3110899429110899430GC17GENIChomozygous111673568
3110901005110901009GGAG5GENIChomozygous130907873
3110901290110901291CT12GENIChomozygous112004321
3110908312110908313TA8GENIChomozygous125865427
3110903300110903301A23GENIChomozygous127918275
3110904918110904919T8GENICpossibly homozygous127918276
3110908956110908956T11GENIChomozygous127918277