chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91712783617127837AC24GENIChomozygous117270154
91712816717128168CG23GENIChomozygous117270155
91713121117131212TC23GENIChomozygous117768280
91713189717131898TA16GENIChomozygous117270157
91713510717135108TC22GENIChomozygous117270158
91713526017135261GC32GENIChomozygous117270159
91713556517135566GA21GENIChomozygous117270160
91713736217137363CT16GENIChomozygous117768282
91713915917139160GA20GENICpossibly homozygous117270162
91714783417147835GT19GENIChomozygous117270163
91715022917150230GA24GENIChomozygous117462723
91715023017150231AG24GENIChomozygous117462724
91715048317150484TC12GENIChomozygous117270164
91715294917152950TA30GENIChomozygous117768284
91715471817154719TC27GENIChomozygous117270169
91715612817156129TC28GENIChomozygous117270170
91715628617156287AG24GENIChomozygous117270171
91715668717156688CT31GENIChomozygous117768286
91716113717161138AG35GENIChomozygous117270173
91716224717162248TC34GENIChomozygous117270174
91716277417162775GA10GENIChomozygous117270175