chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110140024110140025CT7GENIChomozygous51958641
10110140154110140155AG15GENIChomozygous51601062
10110140346110140347A-17GENICpossibly homozygous51601063
10110140427110140428G-3GENIChomozygous51958644
10110140631110140632GC6GENIChomozygous51958647
10110140635110140636AG8GENIChomozygous51601064
10110141328110141342GTCGTCAGTGCTGC--------------1GENIChomozygous52331909
10110142102110142103AC14INTERGENIChomozygous51958653
10110142724110142725A-2INTERGENIChomozygous51774840
10110142859110142860TC11INTERGENIChomozygous51601068
10110145666110145667TC22GENIChomozygous51601069
10110147376110147377TA20GENICpossibly homozygous51958661
10110147657110147658CA21GENIChomozygous51601074
10110147827110147828AC29GENICpossibly homozygous51601075
10110147935110147936GA9GENIChomozygous51958664