chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1273260827273260828CT18GENICpossibly homozygous61224089
1273261581273261583TT--4GENICheterozygous61224090
1273261605273261606AG6GENIChomozygous61224091
1273261811273261812CT11GENICpossibly homozygous61224092
1273262075273262076AAC7GENIChomozygous61224093
1273262993273262994TA9GENICheterozygous61224096
1273262994273262995CG9GENICheterozygous61224097
1273263647273263648GA8GENIChomozygous61224098
1273264227273264228TA8GENIChomozygous61224099
1273267709273267710GA6GENIChomozygous61224103
1273267833273267834AG11GENICpossibly homozygous61224104
1273270637273270638G-16GENIChomozygous61224105