chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77036257970362580TC29GENIChomozygous53956258
77036280170362802TC29GENIChomozygous53956259
77036300270363003A-22GENIChomozygous54444868
77036346570363466GT28GENIChomozygous53956261
77036480870364810GT--8GENIChomozygous53956270
77036662470366625CT26GENIChomozygous53956287
77036729370367294CA21GENIChomozygous54444870
77036739670367397AAT19GENIChomozygous54444872
77036779070367791GC8GENICheterozygous53956306
77036910870369109TC19GENIChomozygous53956310
77036964770369648AG17GENIChomozygous53956313
77036978570369786CA9GENIChomozygous54444874
77036978970369790CA9GENIChomozygous54444876
77036979370369794CA9GENIChomozygous54444878
77036992870369929A-9GENIChomozygous53956315
77037100570371006AAGGACGGAC14GENIChomozygous54444880
77037131670371317CT21GENIChomozygous54444882
77037298370372984TC15GENIChomozygous54444884
77037344170373442TC25GENIChomozygous54444886
77037361070373611TC16GENIChomozygous53956336
77037362470373625TC14GENIChomozygous53956338
77037383170373832TC27GENIChomozygous54444889
77037400370374004G-25GENIChomozygous54444891
77037465970374665ATAAAT------9GENIChomozygous54444893
77037467770374681CTTT----14GENICheterozygous54444895
77037499570374998TTT---12GENIChomozygous54444897
77037514970375150GA23GENIChomozygous54444899
77037559670375597AG5GENIChomozygous54444902
77037595170375952AG7INTERGENIChomozygous54444904
77037640270376403T-11INTERGENICheterozygous54444906
77037653070376531GA22INTERGENIChomozygous54444908
77037698770376988AG25INTERGENICpossibly homozygous54444910