chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135406133135406136CAT---9GENIChomozygous57336952
4135406266135406267TTATACCAGA15GENIChomozygous57336954
4135406268135406269TG15GENIChomozygous58282858
4135406388135406389TA17GENIChomozygous57336956
4135406596135406597CT13GENIChomozygous56937470
4135406921135406922AG15GENIChomozygous57336969
4135407001135407002TTC17GENICheterozygous58282860
4135407028135407029AG17GENICpossibly homozygous57336971
4135407150135407151CT24GENIChomozygous57336973
4135407191135407193AG--17GENIChomozygous56937478
4135407390135407391CA31GENIChomozygous56937486
4135407489135407490AC28GENIChomozygous56937490
4135407589135407590CA27GENIChomozygous56937496
4135407736135407737TTG11GENIChomozygous56937499
4135407742135407743T-10GENIChomozygous56937500
4135407747135407748AC9GENIChomozygous56937501
4135407748135407749AC9GENIChomozygous56937502
4135408544135408545GA31GENIChomozygous57336985