chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101654357816543579TA26GENIChomozygous116738803
101654434216544343GT23GENICpossibly homozygous116738804
101654486116544861T16GENIChomozygous132143412
101654574716545747GAG21GENIChomozygous132143413
101654586416545864CCGCCA18GENIChomozygous132143414
101654661316546614AG19GENIChomozygous116738805
101654769416547695AG20GENIChomozygous116738806
101654783416547835A9GENIChomozygous132143415
101654882616548827GT13GENIChomozygous116860995
101654884116548842GT12GENIChomozygous116738807
101654885216548853TA12GENIChomozygous116738808
101654930316549304GA17GENIChomozygous116738809
101655210416552105C16GENIChomozygous131088460