chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71190506111905062TG3GENIChomozygous53789654
71190557111905572CT31GENIChomozygous53789655
71190564811905649GA29GENIChomozygous53789656
71190578411905785GA25GENIChomozygous53789657
71190618611906187TA7GENIChomozygous53789658
71190618911906190AAGG5GENIChomozygous53789659
71190753711907538AG30GENIChomozygous53789660
71190806911908070AG29GENIChomozygous53789661
71190871211908713GA7GENIChomozygous53789662
71190901711909018AT17GENIChomozygous53789663
71190922811909229T-11GENICpossibly homozygous53789665
71191047611910477AG33GENIChomozygous53789668
71191050811910509CT35GENIChomozygous53789669
71191051911910520CT31GENIChomozygous53789670
71191061711910618GT29GENIChomozygous53789671
71191093811910939AG23GENIChomozygous53789672
71191134511911346TA31GENIChomozygous53789673
71191295111912952CT30GENIChomozygous53789674
71191310711913108GC30GENIChomozygous53789675
71191379111913792CT17GENIChomozygous53789676
71191399511913996GC16GENIChomozygous53789677