chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140571461140571462CCTTTT5GENIChomozygous742621677
7140572424140572425GT10GENICpossibly homozygous618852549
7140572685140572688TTT---14GENICpossibly homozygous742621678
7140572686140572688TT--14GENICheterozygous742621679
7140572952140572953AG7GENIChomozygous618852550
7140573492140573493AG9GENIChomozygous618852551
7140574369140574370AG25GENIChomozygous618852552
7140574482140574483TC18GENIChomozygous618852553
7140574764140574765CT20GENIChomozygous618852554
7140576296140576297CCT10GENIChomozygous742621682
7140576502140576503GA12GENIChomozygous618852555
7140576874140576875AAT4GENIChomozygous742621683
7140577113140577114AAG3GENICheterozygous742621684
7140579414140579415TTCA2GENICheterozygous742621685
7140579436140579437GGAATAAATA1GENIChomozygous742621688
7140580004140580005AACT9GENIChomozygous742621689
7140580850140580851AAGT8GENIChomozygous742621691