chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186877487468774875CT31GENIChomozygous64064148
186877564968775650GA11GENIChomozygous64199123
186877698168776982AG21GENIChomozygous64199124
186877707068777071GT19GENIChomozygous64199125
186877715668777157TC29GENIChomozygous64064193
186877752568777526CT32GENIChomozygous64199126
186878276568782766TA17GENIChomozygous64064244
186878330968783310AC25GENIChomozygous64199127
186878376368783764TC21GENIChomozygous64064269
186878485868784859GA28GENICheterozygous64064272
186878543668785437TA24GENIChomozygous64199128
186878553468785535AG30GENIChomozygous64064278
186878596568785966GT10GENIChomozygous63931258
186878596768785968GT10GENIChomozygous63931260
186878596968785970GT10GENIChomozygous63931262
186878630568786306TC8GENIChomozygous64064289
186878717568787176GA19GENIChomozygous64199129
186878769268787693GT19GENIChomozygous64199130
186878771568787716CT16GENIChomozygous64199131
186878807468788075CA16GENIChomozygous64064313
186878850968788510GC16GENIChomozygous64199133
186878861368788614CT18GENIChomozygous64199134
186878991368789914GA23GENIChomozygous64199135
186878994068789941CT20GENICpossibly homozygous64199136
186879160168791602AG24GENIChomozygous64064349
186879190368791904TA30GENIChomozygous64199137
186879216568792166TC17GENIChomozygous64064352
186879238068792381AG26GENIChomozygous64199138
186879499368794994GT29GENIChomozygous64064371
186879600968796010TG25GENIChomozygous64064373
186879689468796895AG30GENIChomozygous64199139
186879908068799081CT23GENIChomozygous64064396