chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113517014835170149TC14GENIChomozygous50728763
113517079735170798G-2GENIChomozygous50728769
113517126035171261CA7GENIChomozygous50728774
113517135435171355A-20GENIChomozygous50728775
113517219235172193TC23GENICpossibly homozygous50728776
113517570635175707T-20GENICpossibly homozygous51232301
113517733435177335AG15GENIChomozygous50728782
113517977535179776TC18GENICpossibly homozygous50728786
113518386735183868T-16GENICpossibly homozygous50728794
113518404835184049CA26GENIChomozygous50728795
113518491935184920CT19GENIChomozygous50923761
113518568935185690TC30GENICpossibly homozygous51232302
113518761535187616AG21GENICpossibly homozygous50923764
113518789235187893CA12GENIChomozygous51232303
113518853235188534TC--18GENIChomozygous50728806
113518894335188944TC27GENIChomozygous50728808
113518921235189213AG16GENIChomozygous50728809
113518943235189433TC18GENIChomozygous50728810
113518948635189487GA13GENICheterozygous51232304