chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45090247650902477CCA6GENICheterozygous760533815
45093657450936575AAG30GENIChomozygous760533816
45093841850938452TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCA----------------------------------13GENICheterozygous760533817
45093850350938504AATATCTCTAACTGATAAGAAAAGAT9GENICheterozygous760533818
45094277250942773GT10GENIChomozygous655851205
45094277350942774GGTC10GENIChomozygous760533819
45094277650942779GGG---9GENIChomozygous760533820
45094277950942780GT7GENIChomozygous655851206
45094278550942786GGAT13GENIChomozygous760533821
45094278750942788CG13GENIChomozygous655851207
45095170250951703GT14GENIChomozygous655851208
45095170650951707CCT16GENIChomozygous760533822
45095170850951709AAG16GENIChomozygous760533823
45095171750951718CG17GENIChomozygous655851209
45095172050951721T-17GENIChomozygous760533824
45095172550951726C-18GENIChomozygous760533825
45095172650951727CG18GENIChomozygous655851210
45095173050951731AG20GENIChomozygous655851211
45095173250951733TTGTA20GENIChomozygous760533826
45095359050953591A-7GENICheterozygous760533827