chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140571461140571462CCTTTT5GENIChomozygous54262842
7140572424140572425GT10GENICpossibly homozygous54262845
7140572685140572688TTT---14GENICpossibly homozygous54262848
7140572686140572688TT--14GENICheterozygous55315085
7140572952140572953AG7GENIChomozygous54262851
7140573492140573493AG9GENIChomozygous54262853
7140574369140574370AG25GENIChomozygous54262856
7140574482140574483TC18GENIChomozygous54262859
7140574764140574765CT20GENIChomozygous54262862
7140576296140576297CCT10GENIChomozygous54154739
7140576502140576503GA12GENIChomozygous54262865
7140576874140576875AAT4GENIChomozygous54262869
7140577113140577114AAG3GENICheterozygous54262872
7140579414140579415TTCA2GENICheterozygous54154743
7140580004140580005AACT9GENIChomozygous54154745
7140580850140580851AAGT8GENIChomozygous54262876
7140579436140579437GGAATAAATA1GENIChomozygous55016604