chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108264969182649692CT37GENIChomozygous51518112
108264970782649708CA34GENIChomozygous51518113
108264990782649908AT24GENIChomozygous51518114
108265071182650712TC26GENIChomozygous51518115
108265158282651583A-27GENIChomozygous51518116
108265247282652478ACACAC------17GENIChomozygous52506320
108265259082652591AG29GENIChomozygous51992321
108265311482653122GTGTGTGT--------21GENICpossibly homozygous52506322
108265314282653143GA30GENICpossibly homozygous51718561
108265335482653355AATG33GENICpossibly homozygous51718563
108265370382653704TC17GENIChomozygous51518123
108265519482655195TC30GENIChomozygous51518124
108265534582655346AT23GENIChomozygous51518125
108265582982655830CT28GENIChomozygous51518126
108265675982656760TA30GENIChomozygous51518128
108265787682657877GA24GENIChomozygous51518129
108265799082657991TTACAC12GENIChomozygous51518130
108265977482659775TC28GENIChomozygous51518132
108266116682661167CT33GENIChomozygous51992332
108266182682661827GA46GENIChomozygous51992335
108266195882661959TC34GENIChomozygous51992338
108266211682662117GA30GENIChomozygous51992341
108266216882662169AC39GENIChomozygous51992344
108266244782662448GA48GENIChomozygous51992347
108265332382653325TA--33GENICpossibly homozygous53158495