chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8132362793132362794GA12GENIChomozygous52901355
8132362957132362958TTA14GENIChomozygous52901357
8132365445132365446TG21GENIChomozygous52901361
8132365492132365493TC31GENICheterozygous54274620
8132365519132365520TC39GENICheterozygous52901363
8132365526132365527AT38GENICheterozygous52901365
8132365532132365533TA32GENICheterozygous54274622
8132365534132365535CT30GENICheterozygous54274624
8132365535132365536CA30GENICheterozygous54274626
8132365537132365538CA30GENICheterozygous54274628
8132365540132365541CT31GENICheterozygous53067150
8132365552132365553CT35GENICheterozygous52901367
8132365697132365698AC37GENICheterozygous52901369
8132365699132365700CT36GENICheterozygous52901371
8132365711132365712TG36GENICheterozygous52901373
8132365756132365757GA40GENICheterozygous52901375
8132365759132365760CT40GENICheterozygous52901377
8132365780132365781GC35GENICheterozygous52901379
8132365787132365788AT35GENICheterozygous52901381
8132365798132365799AG35GENICheterozygous52901383
8132365801132365802AC35GENICheterozygous52901385
8132365804132365805CT35GENICheterozygous52901387
8132365806132365807AC36GENICheterozygous52901389
8132365854132365855TC36GENICheterozygous54274630
8132365993132365994AG28GENICheterozygous54274632
8132366020132366021TC31GENICheterozygous53184002
8132366033132366034AC33GENICheterozygous53172726
8132366062132366063GA28GENICheterozygous53172728
8132366071132366072CT28GENICheterozygous53172730
8132366080132366081AG36GENICheterozygous53172732
8132366128132366129CA30GENICheterozygous54274634
8132366134132366135CT28GENICheterozygous54274636
8132366140132366141CT27GENICheterozygous54274638
8132366144132366145CT27GENICheterozygous54274640
8132366252132366253CG21GENICheterozygous54274642
8132366254132366255CT21GENICheterozygous54274644
8132366257132366258CT22GENICheterozygous54274646
8132366261132366262GA21GENICheterozygous54274648
8132366266132366267CT21GENICheterozygous54274650
8132366675132366676CA12GENIChomozygous52901395