chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5169112372169112373TC20GENIChomozygous114087635
5169113004169113005AG32GENIChomozygous114087637
5169115300169115301AG22GENICpossibly homozygous114087643
5169115376169115377GA22GENIChomozygous114087645
5169115492169115493GC19GENIChomozygous114087647
5169116064169116065CG13GENIChomozygous114087649
5169116834169116835TG26GENICpossibly homozygous114087651
5169116892169116893GA23GENICpossibly homozygous114087653
5169120090169120091TC25GENIChomozygous114087655
5169120957169120958CT20GENIChomozygous114087657
5169124594169124595GA21GENICpossibly homozygous114087659
5169124839169124840GA23GENICpossibly homozygous114087661
5169126222169126223AG26GENICpossibly homozygous114087665
5169127247169127248TC36GENICpossibly homozygous114087667
5169138902169138903CT25GENIChomozygous114087677
5169140004169140005AG19GENIChomozygous114087679
5169141153169141154GA31GENIChomozygous114087681
5169141656169141657AG24GENIChomozygous114087685
5169145575169145576AG24GENIChomozygous114087687
5169145723169145724CA21GENIChomozygous114087689
5169146433169146434AC19GENIChomozygous114087691
5169149393169149394AT27GENIChomozygous114087693
5169151436169151437AT23GENICpossibly homozygous114087695
5169152739169152740AG33GENIChomozygous114087697