chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71188210811882109CT23GENICpossibly homozygous53789579
71188356911883570CCCTGT9GENICpossibly homozygous53789580
71188588811885889GA12GENICpossibly homozygous53789594
71188591511885916GC19GENIChomozygous53789595
71188596111885962GC7GENIChomozygous53789596
71188597211885973CT9GENICpossibly homozygous53789597
71188703011887031TC12GENIChomozygous53789598
71188776911887770AT21GENIChomozygous53789599
71188779611887797GT12GENICpossibly homozygous53789600
71188858311888584TTAC21GENICpossibly homozygous53789603
71188865411888655CT20GENICpossibly homozygous53789604
71188882411888825GA12GENIChomozygous53789605
71188890011888901AG25GENICpossibly homozygous53789606
71188912511889126GT31GENICpossibly homozygous53789607
71188969111889693CA--17GENIChomozygous53789608
71189064711890648TG15GENIChomozygous53789609
71189146411891465AG21GENIChomozygous53789613
71189177211891773CT17GENIChomozygous53789614
71189185211891853TC22GENICpossibly homozygous53789615
71189197611891977TC22GENIChomozygous53789616