chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5156585050156585051AT11GENICheterozygous55804362
5156587081156587082CA41GENICpossibly homozygous55804363
5156589360156589361GT13GENICheterozygous55804364
5156589363156589364GA14GENICpossibly homozygous55932340
5156589364156589365GT14GENICpossibly homozygous55932342
5156589368156589369TC16GENICpossibly homozygous55804365
5156589370156589371TA15GENICpossibly homozygous55804366
5156594122156594123TTC19GENIChomozygous55804367
5156594133156594134CCCT19GENIChomozygous55804368
5156594137156594138GC26GENIChomozygous55804369
5156597127156597128A-6GENICheterozygous55932346
5156602147156602148CCT28GENIChomozygous55804371
5156606545156606546C-24GENIChomozygous55804372
5156606565156606566T-21GENIChomozygous55804373