chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143517878143517879AG26GENIChomozygous115943991
7143517950143517951GT42GENICpossibly homozygous115943992
7143517979143517980AG34GENIChomozygous115943993
7143519095143519096TC28GENIChomozygous115943994
7143519570143519571CT24GENICpossibly homozygous115943995
7143519781143519782AG15GENIChomozygous115943996
7143520228143520229GA27GENIChomozygous115943997
7143520286143520287AG33GENICpossibly homozygous115943998
7143520320143520321AT31GENIChomozygous115943999
7143520703143520704TG24GENIChomozygous115944000
7143520827143520828GA29GENIChomozygous115944001
7143521277143521278CT23GENICpossibly homozygous115944002