chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105362154253621543GA24GENIChomozygous116887444
105362155353621554TC16GENIChomozygous116887446
105362156953621570AG18GENIChomozygous116887448
105362174053621741CT36GENIChomozygous116887450
105362175053621751GA37GENIChomozygous116887452
105362184453621845CT34GENIChomozygous116887454
105362226153622262CA28GENIChomozygous116887456
105362238553622386CA22GENIChomozygous116887458
105362269453622695CT33GENIChomozygous117011133
105362334753623348CT26GENIChomozygous117011134
105362343653623437CA25GENIChomozygous116887462
105362347353623474GA30GENIChomozygous117011135
105362381653623817TC29GENIChomozygous116887464
105362393453623935AC31GENIChomozygous116887466
105362397153623972CG20GENIChomozygous116887468
105362400253624003CT26GENIChomozygous116887470
105362407953624080CG25GENIChomozygous116887472
105362415753624158AG23GENIChomozygous116887474
105362703253627033CT23GENIChomozygous116887482
105362797453627975CT36GENIChomozygous116887484
105362806953628070GA32GENIChomozygous116887486
105362909253629093TC29GENIChomozygous116887490
105362910753629108AG35GENIChomozygous116887492
105363266053632661GA21GENIChomozygous117011136
105363301353633014TG25GENIChomozygous117011137
105363373653633737AT32GENIChomozygous116887502
105363373753633738GA31GENIChomozygous116887504
105363417153634172GA17GENIChomozygous117011138
105363463053634631GA35GENIChomozygous116887506
105363490353634904AT30GENIChomozygous116887510
105363497853634979GA27GENIChomozygous117011139
105363561753635618GT28GENIChomozygous117011140
105363569453635695CT27GENIChomozygous116887512
105363581053635811CT22GENIChomozygous117011141
105363627653636277AG25GENIChomozygous116887516
105363632153636322TC27GENIChomozygous116933691
105363674953636750AG21GENIChomozygous116887518
105363679453636795CT21GENIChomozygous117011142
105363776153637762AC30GENIChomozygous116887520
105363904153639042CA35GENIChomozygous116887522
105364079453640795CT28GENIChomozygous116887524
105364177453641775GA41GENIChomozygous117011143