chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1219083495219083496TC31GENIChomozygous120515549
1219083496219083497CT31GENIChomozygous120490544
1219083782219083783A36GENIChomozygous127484442
1219083794219083795A39GENIChomozygous127484443
1219083797219083798AT39GENIChomozygous108540171
1219083804219083805TC37GENIChomozygous109537938
1219083805219083806AT37GENIChomozygous120490545
1219088055219088055CTTTAGA29GENIChomozygous127484445
1219095831219095831A26GENIChomozygous127484449
1219101748219101748AT41GENIChomozygous127484452
1219101749219101749T42GENIChomozygous127484453
1219111982219111983CA38GENIChomozygous108540248
1219088095219088095T32GENIChomozygous130217100