chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148901807589018076AG45GENIChomozygous48824761
148901995489019955GA30GENIChomozygous48824763
148902054589020553CGCGCGCA--------14GENICpossibly homozygous48824765
148902207889022079CCCA37GENIChomozygous48824767
148902298989022991AC--3GENICheterozygous48824769
148902307189023075TTGT----6GENIChomozygous48824771
148902386989023870GGAC23GENICpossibly homozygous48824773
148902430789024308CT25GENICpossibly homozygous48824775
148902441289024413AC32GENICheterozygous48824777
148902441489024415GC32GENICheterozygous48824779
148902760189027602CCT28GENICpossibly homozygous48824781
148903436489034365CCATCTATCT6GENICheterozygous48824783
148904008989040090CCAA26GENICheterozygous48824785
148904008989040090CCA26GENICpossibly homozygous48824787
148904686989046870G-25GENIChomozygous48824789
148904892789048928TA40GENICpossibly homozygous48824791
148904948889049489GGCA20GENICheterozygous48824793
148905014589050146CCT22GENIChomozygous48824795