chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184073486340734864GA22GENIChomozygous110329840
184074408140744082AT19GENIChomozygous110329844
184074764540747646AG31GENIChomozygous110329848
184074854640748547AC23GENIChomozygous110329852
184074888440748885TC28GENIChomozygous110329854
184074943840749439AG15GENIChomozygous110728679
184075064640750647CG26GENIChomozygous110728681
184075077940750780CT5GENIChomozygous110728683
184075089240750893GA18GENIChomozygous110728685
184075118040751181TG8GENIChomozygous110329860
184075817740758178AC17GENIChomozygous110728687
184075910740759108TC23GENIChomozygous110728689
184076903340769034GC22GENIChomozygous110728691
184076905840769059GA22GENIChomozygous110728693
184077117040771171GA17GENIChomozygous110728695
184077723640777237GC15GENIChomozygous110329868
184077755840777559GA22GENIChomozygous110728697
184078344340783444TG27GENIChomozygous110728699
184078487740784878GA13GENIChomozygous110463702
184078641840786419TG3GENIChomozygous110329876
184078866740788668CT11GENIChomozygous110463704
184079515240795153TA12GENIChomozygous110728701
184079693440796935TC16GENIChomozygous110728703