chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5173340455173340456AG6GENIChomozygous982310442
5173341068173341069CT18GENIChomozygous982310443
5173342937173342938GC7GENIChomozygous982310444
5173344718173344719CT20GENIChomozygous982310445
5173345388173345389GA25GENIChomozygous982310446
5173345461173345462GA21GENIChomozygous982310447
5173345467173345468GA22GENIChomozygous982310448
5173345503173345504CT15GENIChomozygous982310449
5173347147173347148AG14GENIChomozygous982310450
5173347178173347179TC16GENIChomozygous982310451
5173347309173347310TA25GENIChomozygous982310452
5173347489173347490TC21GENIChomozygous982310453
5173347683173347684AG13GENIChomozygous982310454
5173348062173348063GT14GENIChomozygous982310455
5173348303173348304GA18GENIChomozygous982310456
5173348372173348373AG9GENIChomozygous982310457
5173348932173348933GA28GENIChomozygous982310458
5173349421173349422TA18GENIChomozygous982310459
5173349703173349704AG19GENIChomozygous982310460
5173349906173349907AC21GENIChomozygous982310461
5173350440173350441GA24GENIChomozygous982310462
5173352655173352656CT15GENIChomozygous982310463
5173352692173352693AG14GENIChomozygous982310464
5173352901173352902TC18GENIChomozygous982310465
5173354070173354071GA13GENIChomozygous982310466