chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77036257970362580TC23GENIChomozygous53956258
77036280170362802TC17GENIChomozygous53956259
77036300270363003A-27GENIChomozygous54444868
77036346570363466GT19GENIChomozygous53956261
77036471070364711CCA5GENICheterozygous55026953
77036480870364812GTGT----1GENIChomozygous54981549
77036662470366625CT17GENIChomozygous53956287
77036729370367294CA22GENIChomozygous54444870
77036739670367397AATT12GENIChomozygous54656818
77036910870369109TC14GENIChomozygous53956310
77036964770369648AG18GENIChomozygous53956313
77036978170369782CCAAA4GENIChomozygous54981554
77036978570369786CA4GENIChomozygous54444874
77036978970369790CA1GENIChomozygous54444876
77036992870369929A-7GENIChomozygous53956315
77037100570371006AAGGACGGAC9GENIChomozygous54444880
77037131670371317CT27GENIChomozygous54444882
77037298370372984TC14GENIChomozygous54444884
77037344170373442TC13GENIChomozygous54444886
77037355770373560GGG---1GENIChomozygous54981556
77037362470373625TC16GENIChomozygous53956338
77037383170373832TC23GENIChomozygous54444889
77037400370374004G-16GENICpossibly homozygous54444891
77037465970374665ATAAAT------1GENIChomozygous54444893
77037499570374998TTT---9GENICheterozygous54444897
77037514970375150GA12GENIChomozygous54444899
77037559670375597AG3GENIChomozygous54444902
77037589970375900GGGTGGTGGGCGGGGC1INTERGENIChomozygous54981560
77037595170375952AG4INTERGENIChomozygous54444904
77037640270376403T-9INTERGENICpossibly homozygous54444906
77037640470376409TGTGT-----11INTERGENICheterozygous54981561
77037653070376531GA21INTERGENIChomozygous54444908
77037698770376988AG18INTERGENIChomozygous54444910