chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81336581813365819CT27GENICpossibly homozygous116924120
81336601113366012CT13GENIChomozygous116924121
81336634513366346TC31GENIChomozygous116924123
81336847913368480TC21GENIChomozygous116924125
81336849213368493GA18GENIChomozygous116924127
81337043813370439GA19GENIChomozygous116924129
81337064813370649CT21GENIChomozygous116924131
81337100813371009AG22GENIChomozygous116924133
81337162113371622TG14GENIChomozygous116924135
81337162513371626TC15GENIChomozygous116924136
81337180713371808GA18GENIChomozygous116924138
81337230913372310TC14GENIChomozygous116924140
81337175413371774CTTGGAACTTCTAGGAGGCA13GENIChomozygous131041600
81337264513372645CACT20GENIChomozygous131041601
81336721513367219CACT16GENIChomozygous131041597
81336928613369288CA18GENIChomozygous131041598
81337282513372826GC17GENIChomozygous116924142
81337307413373075GA33GENIChomozygous116924144
81337347513373476TC28GENIChomozygous116924146
81337375113373752CT26GENIChomozygous116924147
81337446913374470CT16GENIChomozygous116924149
81337512513375126TA29GENIChomozygous116924151
81337517713375178TA17GENIChomozygous116924153
81337526213375263TC19GENIChomozygous116924155