chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5156587081156587082CA16GENICpossibly homozygous55804363
5156594122156594123TTC4GENICheterozygous55804367
5156594133156594134CCCT1GENIChomozygous55804368
5156594137156594138GC1GENIChomozygous55804369
5156596372156596373AAAC17GENICheterozygous55804370
5156602147156602148CCT9GENIChomozygous55804371
5156606545156606546C-12GENIChomozygous55804372
5156606565156606566T-9GENIChomozygous55804373