chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77036257970362580TC25GENIChomozygous53956258
77036280170362802TC28GENIChomozygous53956259
77036300270363003A-21GENIChomozygous54444868
77036346570363466GT25GENIChomozygous53956261
77036480870364810GT--8GENIChomozygous53956270
77036662470366625CT16GENIChomozygous53956287
77036729370367294CA24GENIChomozygous54444870
77036739670367397AAT23GENIChomozygous54444872
77036910870369109TC34GENIChomozygous53956310
77036964770369648AG28GENIChomozygous53956313
77036978570369786CA13GENIChomozygous54444874
77036978970369790CA12GENIChomozygous54444876
77036979370369794CA14GENIChomozygous54444878
77036992870369929A-16GENICheterozygous53956315
77037100570371006AAGGACGGAC10GENIChomozygous54444880
77037131670371317CT34GENIChomozygous54444882
77037298370372984TC35GENIChomozygous54444884
77037344170373442TC25GENICpossibly homozygous54444886
77037361070373611TC19GENIChomozygous53956336
77037362470373625TC22GENIChomozygous53956338
77037383170373832TC27GENIChomozygous54444889
77037400370374004G-20GENIChomozygous54444891
77037465970374665ATAAAT------11GENIChomozygous54444893
77037467770374681CTTT----15GENICheterozygous54444895
77037499570374998TTT---9GENIChomozygous54444897
77037514970375150GA23GENIChomozygous54444899
77037559670375597AG34GENIChomozygous54444902
77037595170375952AG9INTERGENIChomozygous54444904
77037640270376403T-28INTERGENICheterozygous54444906
77037653070376531GA33INTERGENIChomozygous54444908
77037698770376988AG24INTERGENIChomozygous54444910