chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148901807589018076AG66GENICpossibly homozygous48824761
148901995489019955GA51GENIChomozygous48824763
148902054589020553CGCGCGCA--------7GENICpossibly homozygous48824765
148902207889022079CCCA38GENIChomozygous48824767
148902298989022991AC--7GENIChomozygous48824769
148902307189023075TTGT----5GENICheterozygous48824771
148902386989023870GGAC28GENICpossibly homozygous48824773
148902430789024308CT39GENICpossibly homozygous48824775
148902760189027602CCT24GENIChomozygous48824781
148903436489034365CCTATCTATCT18GENICheterozygous49028362
148903436489034365CCATCTATCT18GENICpossibly homozygous48824783
148904008989040090CCA25GENICheterozygous48824787
148904112389041124CG78GENICheterozygous49028368
148904647989046480TC17GENICheterozygous49028372
148904648689046487TC12GENICheterozygous49028374
148904686989046870G-29GENIChomozygous48824789
148904892789048928TA36GENICpossibly homozygous48824791
148904948889049489GGCA21GENICpossibly homozygous48824793
148905014589050146CCT28GENICpossibly homozygous48824795