chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148901775489017762GTGTGTGT--------4GENICheterozygous49317203
148901775689017762GTGTGT------4GENICheterozygous49317204
148901807589018076AG21GENIChomozygous48824761
148901995489019955GA22GENIChomozygous48824763
148902054589020553CGCGCGCA--------6GENIChomozygous48824765
148902207889022079CCCA25GENIChomozygous48824767
148902298989022991AC--7GENICpossibly homozygous48824769
148902307189023075TTGT----9GENICheterozygous48824771
148902307189023079TTGTGTGT--------9GENICheterozygous49327822
148902386989023870GGAC15GENICpossibly homozygous48824773
148902430789024308CT29GENIChomozygous48824775
148902445989024460TTCTCTC17GENICheterozygous49317205
148902674789026755TGTGTGTG--------11GENICheterozygous49317206
148902674989026755TGTGTG------11GENICheterozygous49317207
148902760189027602CCT11GENICheterozygous48824781
148903436489034365CCATCTATCT9GENICpossibly homozygous48824783
148903436489034365CCATCT9GENICheterozygous49425059
148904008989040090CCAA20GENICheterozygous48824785
148904008989040090CCA20GENICheterozygous48824787
148904686989046870G-23GENIChomozygous48824789
148904892789048928TA18GENIChomozygous48824791
148904948889049489GGCA9GENICheterozygous48824793
148904948889049489GGCACA9GENICheterozygous49397725
148905014589050146CCT16GENIChomozygous48824795