chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105598580955985810CT13GENIChomozygous51654123
105598708055987081TG37GENICheterozygous52194487
105598843355988434GA16GENIChomozygous51654125
105599021855990219GA9GENIChomozygous51654127
105599046955990470GA9GENIChomozygous51654129
105599087255990874CC--4GENICheterozygous51890890
105599087355990874C-4GENICheterozygous51459962
105599136555991366AG13GENIChomozygous51654131
105599222055992222TT--6GENICheterozygous51654135
105599222155992222T-6GENICheterozygous51459963
105599236455992365CCTT25GENIChomozygous51654137
105599274455992745CT21GENICheterozygous51890893
105599314555993146AAC17GENIChomozygous51890896
105599392055993921CT17GENIChomozygous51654141
105599422855994229A-22GENIChomozygous51459965
105599460555994606TTAATAATA3GENIChomozygous51890899
105599496455994965AG23GENIChomozygous51654147
105599532255995323AAT21GENIChomozygous51654149
105599542955995430GA22GENIChomozygous51890902
105599544555995446AC18GENICpossibly homozygous51654151
105599581155995812CG24GENIChomozygous51654155
105599589055995891TC24GENIChomozygous51654157
105599665555996656CCT16GENICpossibly homozygous51654161
105599772455997726TT--2GENICheterozygous52194489
105599772555997726T-2GENICheterozygous51654166
105599840855998409AG24GENIChomozygous51654168