chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71506699415066995GA19GENIChomozygous115576123
71506719315067194GA30GENIChomozygous116115333
71506728215067283GA47GENIChomozygous116115334
71506741515067416TC55GENIChomozygous115576125
71506756815067569TC38GENIChomozygous115576126
71506767115067672CT27GENIChomozygous116115335
71506788815067889CA27GENIChomozygous115576128
71506821415068215GA34GENIChomozygous116115336
71506828415068285CT30GENIChomozygous116115337
71506920015069201AC33GENIChomozygous116115338
71507009715070098GA32GENIChomozygous116115339
71507026315070264TC33GENIChomozygous115576133
71507074815070749GA39GENIChomozygous116115340
71507087515070876AG32GENIChomozygous115576136
71507102415071025AG28GENIChomozygous115576137
71507105015071051AG26GENIChomozygous115576138
71507298715072988TG27GENIChomozygous116115344
71507304115073042GA29GENIChomozygous116115345
71507340515073406GA29GENIChomozygous116115346
71507350715073508GA21GENIChomozygous116115347
71507428915074290AT20GENIChomozygous115576146
71507452115074522AG23GENIChomozygous115576147
71507484515074846GC33GENIChomozygous115576148
71507525115075252GT31GENICpossibly homozygous115576149
71507541715075418CG33GENIChomozygous115576150
71507560015075601TC30GENIChomozygous115576151
71507578815075789TC27GENIChomozygous115576152
71507598615075987CA24GENIChomozygous115576153
71507599815075999TC24GENIChomozygous115576154
71507617315076174AC26GENIChomozygous115576155
71507623315076234TC32GENIChomozygous115576156
71507650515076506CG21GENIChomozygous115576159
71507699715076998AG34GENIChomozygous115576161
71507713115077132TC27GENIChomozygous115576162
71507720015077201TA37GENIChomozygous115576163
71507741715077418AG37GENIChomozygous115576164
71507864715078648GA35GENIChomozygous115576166
71507915715079158CG24GENIChomozygous116115349
71507938115079382GA34GENIChomozygous115576167