chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
44493630644936307CT60GENICheterozygous112620823
44493762844937629AT17GENIChomozygous112620825
44493762944937630GC17GENIChomozygous112620827
44493763644937637AC20GENIChomozygous112620829
44493955244939553TA18GENIChomozygous112620831
44493955344939554CG18GENIChomozygous112620833
44493955844939559GA18GENIChomozygous112620835
44493959344939594TC15GENICpossibly homozygous112620837
44493959844939599AG13GENIChomozygous112620839
44494616744946168TG29GENICpossibly homozygous112620841
44494821244948213AG38GENIChomozygous112620843
44495462544954626AG21GENICpossibly homozygous112620845
44495538544955386GT39GENICpossibly homozygous112620847
44496445444964455AG33GENIChomozygous112620849
44496476844964769GA15GENICpossibly homozygous112620851
44496721944967220GC22GENIChomozygous112620853
44496762444967625TA49GENIChomozygous112620855
44496957144969572TC40GENIChomozygous112620857