chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3111013932111013933CG21GENIChomozygous966404892
3111014657111014658TC20GENIChomozygous966404893
3111015014111015015GA8GENICpossibly homozygous966404894
3111015906111015907TA30GENIChomozygous966404895
3111015952111015953AG39GENIChomozygous966404896
3111016316111016317GC24GENIChomozygous966404897
3111017073111017074AG24GENIChomozygous966404898
3111017337111017338TC26GENIChomozygous966404899
3111017673111017674AG19GENIChomozygous966404900
3111018259111018260GA18GENIChomozygous966404901
3111018920111018921CT10GENIChomozygous966404902
3111021557111021558AG26GENIChomozygous966404903
3111021590111021591GA21GENIChomozygous966404904