chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1273260827273260828CT10GENIChomozygous61224089
1273261581273261583TT--9GENIChomozygous61224090
1273261605273261606AG12GENIChomozygous61224091
1273261811273261812CT8GENIChomozygous61224092
1273262075273262076AAC4GENIChomozygous61224093
1273262370273262371CCTTT5GENIChomozygous61224094
1273262656273262657T-2GENIChomozygous61224095
1273262993273262994TA7GENIChomozygous61224096
1273262994273262995CG7GENIChomozygous61224097
1273263647273263648GA6GENIChomozygous61224098
1273264227273264228TA8GENIChomozygous61224099
1273265255273265256GGTTT3GENICheterozygous61224101
1273265255273265256GGTTTTT3GENICheterozygous61646276
1273265979273265980AATT10GENIChomozygous61224102
1273267709273267710GA5GENIChomozygous61224103
1273267833273267834AG9GENIChomozygous61224104
1273270637273270638G-11GENIChomozygous61224105