chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31806249118062492TC16GENIChomozygous143019898
31806825818068259AG25GENIChomozygous143019899
31806831918068320GA24GENIChomozygous143019900
31806911118069112CT16GENIChomozygous143019901
31807043918070440AT11GENIChomozygous143019902
31807048818070489AT12GENIChomozygous143019903
31807053218070533AG11GENIChomozygous143019904
31807170518071706AG27GENIChomozygous143019905
31807202218072023AG5GENIChomozygous136647282
31807223918072240GA15GENIChomozygous143019906
31807290318072904TC14GENIChomozygous143019907
31807297518072976GA10GENIChomozygous143019908
31807429518074296GT21GENIChomozygous143019909
31807457418074575AG27GENIChomozygous136647283
31807489918074900CG4GENIChomozygous143019910
31807491318074916CAG1GENIChomozygous143000606
31807203618072036GGAGGGAA6GENIChomozygous143000603
31807490218074902GGC4GENIChomozygous143000604
31807490818074908AG3GENIChomozygous143000605
31807492918074933CCGA1GENIChomozygous143000607
31807493718074937TAA1GENIChomozygous143000608
31807494118074947CCTGAG1GENIChomozygous143000609
31807551418075515GA24GENIChomozygous143019911
31807554318075544GA19GENIChomozygous143019912
31807557718075578AG15GENIChomozygous143019913
31807618418076185GA16GENIChomozygous136647284
31807939018079393GAA21GENIChomozygous136550666
31807653618076537CA22GENIChomozygous136647285
31807665118076652AG16GENIChomozygous136647286
31807887318078874GA26GENIChomozygous136647287
31807665718076657G17GENIChomozygous136550665
31808008718080088CT22GENIChomozygous136647288
31808031218080313CT20GENIChomozygous136647289
31808046518080466TC21GENIChomozygous136647290
31808088218080883GA14GENIChomozygous136647291