chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1128212340128212341CT23GENIChomozygous108224819
1128212349128212350GA25GENIChomozygous108224821
1128219958128219959AC4GENIChomozygous120848074
1128220016128220017TC6GENIChomozygous108224823
1128220017128220018GA6GENIChomozygous108224825
1128220443128220444TG11GENIChomozygous108742464
1128220444128220445GT10GENIChomozygous120473337
1128220802128220803CA15GENIChomozygous108224829
1128220831128220832GA18GENIChomozygous108224831
1128220989128220990GC13GENIChomozygous120485695
1128231249128231250GC9GENIChomozygous108224840
1128232001128232002GA21GENIChomozygous120473338
1128232120128232121GC15GENIChomozygous120473339
1128232193128232194GT11GENIChomozygous108224842
1128232235128232236GC8GENIChomozygous108224844
1128233176128233177TA17GENIChomozygous108224854
1128233467128233468GC13GENIChomozygous108224856
1128234686128234687CT11GENICpossibly homozygous108224858
1128255381128255382CT22GENIChomozygous120485696
1128255382128255383TC22GENIChomozygous120485697
1128256194128256195CG21GENICpossibly homozygous108224866
1128272337128272338TC13GENIChomozygous108224870
1128285238128285239GT6GENIChomozygous108224874
1128294507128294508TC11GENIChomozygous108224876
1128295672128295673CT10GENIChomozygous108224878
1128299640128299641CT18GENIChomozygous120473340
1128309764128309765GC13GENICheterozygous120848075
1128299639128299640TC18GENIChomozygous109137238
1128338901128338902CT12GENIChomozygous108224918