chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105540108755401088AG10GENIChomozygous51459553
105540215855402159GA5GENIChomozygous52561751
105540753955407540AAT6INTERGENICheterozygous52158956
105540762255407623AATCT6INTERGENICheterozygous51889790
105540891055408911CT20INTERGENICpossibly homozygous51459555
105541359955413600GA26INTERGENICpossibly homozygous52561754
105541571855415719TC21INTERGENIChomozygous51459560
105541785455417855TC18INTERGENICpossibly homozygous52561757
105542323755423238T-4INTERGENIChomozygous52561760
105542330255423303CT1INTERGENIChomozygous52561763
105542371655423717A-1INTERGENIChomozygous51889872
105542704055427041AG19GENIChomozygous51459574
105543405055434051TC15GENIChomozygous51889883
105543455155434552TC14GENICheterozygous51459577
105543585155435852CT30GENICpossibly homozygous52561766
105543672655436727AT4GENICheterozygous52561769
105543672755436728GA4GENICheterozygous52561772
105543855955438560GA31GENICpossibly homozygous52561775
105543997655439977GA24INTERGENIChomozygous52561778
105544079255440793GC18INTERGENIChomozygous52561781
105544631755446318GT4INTERGENIChomozygous52561784
105544648155446482TC10INTERGENICpossibly homozygous51459589
105544831755448318TA1GENIChomozygous51459590
105544860355448604CT7GENICpossibly homozygous51459591
105544880055448801GA25GENICpossibly homozygous52561787