chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141058205010582051TC18GENICpossibly homozygous113338311
141058238410582385CA10GENIChomozygous113338313
141058276610582767GT7GENIChomozygous113338315
141058353110583532CG10GENIChomozygous113338317
141058532910585330AT14GENIChomozygous113338318
141058579310585794GA14GENIChomozygous113338320
141058649110586492CT9GENIChomozygous113338322
141058652610586527TC9GENIChomozygous113338324
141058702210587023CT11GENIChomozygous113338326
141058793010587931TC16GENIChomozygous113338328
141058805110588052GA17GENIChomozygous113338330
141058813010588131GC16GENIChomozygous113338332
141058887610588877CT14GENIChomozygous113338334
141058963110589632TA15GENIChomozygous113338338
141059001010590011GA15GENIChomozygous113338340
141059074610590747CT14GENIChomozygous113338342
141059081910590820CT8GENIChomozygous113338344
141059091110590912TC21GENIChomozygous113338346
141059107410591075CT17GENIChomozygous113338348
141059109410591095CA16GENIChomozygous113338350
141059221310592214TC12GENIChomozygous113338352
141059238210592383CT6GENIChomozygous113338354
141059274110592742CA5GENIChomozygous113338356
141059303010593031GT12GENIChomozygous113338358
141059388510593886GA18GENIChomozygous113338360
141059401210594013CT11GENIChomozygous113338362
141059413010594131GA18GENIChomozygous113338364
141059583810595839TC9GENIChomozygous113338365
141059630510596306GC12GENIChomozygous113338369
141059344110593442GT12GENIChomozygous118675781
141058628210586283GA4GENICheterozygous113783748
141058783210587833CT7GENIChomozygous113574522
141059647010596471CT17GENIChomozygous113338371
141059730210597303GA14GENIChomozygous113338375
141059766210597663AG5GENIChomozygous113926018
141059781310597814GC6GENIChomozygous113338377
141059794210597943GA22GENIChomozygous113338379
141059809510598096AC14GENIChomozygous113338381
141059865910598660AT20GENICpossibly homozygous113338383
141059870810598709GA23GENIChomozygous113338385
141060009810600099TG13GENIChomozygous113338387