chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101459043114590432AG14GENIChomozygous51329676
101459107714591078AAT4GENIChomozygous51329677
101459130714591308CT19GENIChomozygous51329679
101459181714591818TC16GENICpossibly homozygous51329680
101459202314592024CT26GENICpossibly homozygous51329681
101459399514593996CA2GENIChomozygous51329685
101459407014594071AG23GENICpossibly homozygous51329686
101459469614594697TC17GENICpossibly homozygous51329688
101459513814595139GA25GENICpossibly homozygous51329689
101459564814595649GA11GENICheterozygous51329690
101459692414596925GA23GENICpossibly homozygous51329692
101459726014597261GT14GENIChomozygous51329693
101459762414597625CT25GENICpossibly homozygous51329695
101460026014600261CT29GENIChomozygous51329699
101460143514601436CT14GENIChomozygous51329701
101460366514603666TC25GENICpossibly homozygous51329702
101460372514603726TG8GENIChomozygous51329704
101460419614604197TTG3GENIChomozygous51329706