chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105540108755401088AG12GENIChomozygous51459553
105540564155405642GA15INTERGENIChomozygous51459554
105540762255407623AATCT20INTERGENIChomozygous51889790
105540891055408911CT18INTERGENIChomozygous51459555
105541571855415719TC10INTERGENIChomozygous51459560
105540215855402159GA22GENIChomozygous52561751
105541359955413600GA14INTERGENIChomozygous52561754
105541785455417855TC15INTERGENIChomozygous52561757
105540613655406137GA15INTERGENIChomozygous53527584
105541026555410266T-11INTERGENIChomozygous53527586
105541459955414600CCA10INTERGENIChomozygous52800833
105542136055421361GGT8GENIChomozygous51459567
105542323755423238T-14INTERGENIChomozygous52561760
105542330255423303CT16INTERGENIChomozygous52561763
105542704055427041AG16GENIChomozygous51459574
105543405055434051TC11GENIChomozygous51889883
105543455155434552TC8GENIChomozygous51459577
105543585155435852CT13GENIChomozygous52561766
105543672655436727AT7GENIChomozygous52561769
105543672755436728GA7GENIChomozygous52561772
105543806155438062TC14GENIChomozygous53527588
105543855955438560GA14GENIChomozygous52561775
105543997655439977GA12INTERGENIChomozygous52561778
105544079255440793GC12INTERGENIChomozygous52561781
105544631755446318GT20INTERGENIChomozygous52561784
105544648155446482TC14INTERGENIChomozygous51459589
105544831755448318TA12GENIChomozygous51459590
105544860355448604CT17GENIChomozygous51459591
105544880055448801GA13GENIChomozygous52561787
105545414055454141GA30INTERGENIChomozygous53527590