chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18216737882167379AC39GENIChomozygous108877541
18216759482167595CG43GENIChomozygous108877542
18216837982168384GATCC41GENIChomozygous132527539
18216774282167751TTTTCTTTT25GENIChomozygous132527536
18216779482167795T31GENIChomozygous132527537
18216782182167821A36GENIChomozygous132527538
18216865582168656TC28GENIChomozygous108877543
18216898782168988AG31GENIChomozygous108877544
18216902682169027AG35GENIChomozygous108877545
18216920182169202TC39GENICpossibly homozygous108877546
18217011382170114CT42GENIChomozygous108877547
18217057082170571TC37GENIChomozygous108877548
18217203482172035CT22GENIChomozygous108877549