chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87915955379159554TC17GENICpossibly homozygous117145558
87915961379159614TC22GENIChomozygous116523619
87915961579159616TA22GENIChomozygous116523621
87921343579213436GA11GENICheterozygous117145559
87922836779228368AG6GENIChomozygous117046852
87922913979229140AG22GENIChomozygous117145560
87923693379236934AG17GENIChomozygous117145561
87924083679240837GA15GENICheterozygous116523623
87924550079245501CT14GENIChomozygous117145562
87924701979247020AG7GENIChomozygous117145563
87925110679251107GA11GENIChomozygous117145564
87925118479251185GA20GENIChomozygous117145565
87925134379251344CA13GENICpossibly homozygous116523625
87925144379251444GA9GENIChomozygous117145566
87925374379253744AC9GENIChomozygous117145567
87925536079255361GT6GENIChomozygous117145568
87925619879256199AT13GENIChomozygous117145569
87925901779259018GA16GENIChomozygous117145570
87926497779264978AC23GENIChomozygous117145571
87926743179267432GA15GENIChomozygous117145572
87927077779270778AC29GENIChomozygous117145573
87927092479270925GA21GENICheterozygous117145574
87927172779271728TC19GENIChomozygous117145575
87927239779272398TA13GENICpossibly homozygous117145576
87927248879272489AG17GENIChomozygous117145577
87927318379273184AG41GENIChomozygous117145578
87927370179273702TC23GENIChomozygous116971455
87927435079274351GA10GENIChomozygous117046857