chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157554895157554896CT20GENIChomozygous112906644
4157555371157555372TC7GENIChomozygous112906646
4157555466157555467TG12GENIChomozygous112906648
4157555979157555980TC6GENICheterozygous119443440
4157555980157555981TC4GENICheterozygous119317689
4157556617157556618TC15GENIChomozygous112906650
4157557371157557372TC11GENIChomozygous112906652
4157557740157557741AG7GENIChomozygous113308129
4157558488157558489AC15GENIChomozygous112906654
4157558564157558565GA13GENIChomozygous112906656
4157558723157558724TG8GENIChomozygous112906658
4157558756157558757AT18GENIChomozygous112906660
4157559013157559014AG21GENIChomozygous112906662
4157559416157559417AG18GENIChomozygous112906664
4157559933157559934CA6GENICheterozygous126150681
4157560549157560550AG15GENIChomozygous112906666
4157562967157562968GC23GENIChomozygous112906668