chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1219079376219079377T12GENICheterozygous129845046
1219083495219083496TC8GENIChomozygous120515549
1219083496219083497CT8GENIChomozygous120490544
1219083782219083783A7GENIChomozygous127484442
1219083794219083795A8GENIChomozygous127484443
1219083797219083798AT8GENIChomozygous108540171
1219083805219083806AT8GENIChomozygous120490545
1219088055219088055CTTTAGA18GENIChomozygous127484445
1219095831219095831A9GENIChomozygous127484449
1219101748219101748AT17GENIChomozygous127484452
1219101749219101749T17GENIChomozygous127484453
1219083804219083805TC8GENIChomozygous109537938
1219088095219088095T16GENIChomozygous130217100