chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135405632135405633TG5GENIChomozygous59244633
4135406133135406136CAT---7GENICpossibly homozygous57336952
4135406388135406389TA10GENIChomozygous57336956
4135406596135406597CT11GENIChomozygous56937470
4135406921135406922AG12GENICpossibly homozygous57336969
4135407001135407002TTC15GENICheterozygous58282860
4135407028135407029AG11GENICpossibly homozygous57336971
4135407150135407151CT16GENIChomozygous57336973
4135407191135407193AG--5GENIChomozygous56937478
4135407390135407391CA18GENICpossibly homozygous56937486
4135407489135407490AC20GENICpossibly homozygous56937490
4135407736135407737TTG7GENICheterozygous56937499
4135407742135407743T-5GENICheterozygous56937500
4135408544135408545GA20GENICpossibly homozygous57336985