chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107999151379991514CT15GENIChomozygous138831078
107999227579992276GA60GENIChomozygous138831079
107999321679993217CT50GENIChomozygous138831080
107999397479993974GAAC30GENICpossibly homozygous138693288
107999397779993978TC30GENICpossibly homozygous138831081
107999449179994492GA53GENIChomozygous138831082
107999484379994848CTCAC65GENIChomozygous138693289
107999516279995163AG54GENIChomozygous138831083
107999544079995441GA47GENIChomozygous138831084
107999590979995910AG42GENIChomozygous138831085
107999610579996106AG54GENIChomozygous138831086
107999715779997158AG15GENIChomozygous138831087
107999716079997160A15GENIChomozygous138693290
107999716279997162AGGAGGAGGAGGAAGAA15GENIChomozygous138693291
107999757379997573T45GENIChomozygous138693292
107999807279998073CT33GENIChomozygous138831088
107999852579998525TCTCCTATCCTG34GENIChomozygous138693293
107999855579998556AG35GENIChomozygous138831089
107999924179999242TC47GENIChomozygous138831090
107999949079999491TA31GENIChomozygous138831091
108000006380000063C50GENIChomozygous138693294
108000123280001233CT64GENIChomozygous138831092
108000362780003627AG63GENIChomozygous138693295
108000386080003861AC57GENIChomozygous138831093
108000404480004045TC56GENIChomozygous138831094
108000594980005950TC48GENIChomozygous138831095
108000737680007377CT57GENIChomozygous138831096
108001088880010889AG44GENIChomozygous138831097
108001270980012710CT36GENIChomozygous138831098
108001612380016124TC49GENIChomozygous138831099
108001719480017195GA42GENIChomozygous138831100