chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X107538034107538036AG7GENIChomozygous129777101
X107538048107538049G6GENIChomozygous129777102
X107538079107538080C3GENIChomozygous129777103
X107538084107538085A3GENIChomozygous129777104
X107538190107538191A3GENIChomozygous129777105
X107538212107538213A6GENIChomozygous129777106
X107538240107538240AAG7GENIChomozygous129777107
X107538246107538247C7GENIChomozygous129777108
X107538252107538252A7GENIChomozygous129777109
X107538273107538274C9GENIChomozygous129777110
X107538323107538324A10GENIChomozygous129777111
X107540111107540113TT4GENIChomozygous129777112
X107540116107540117T4GENIChomozygous129777113
X107540133107540135GG5GENIChomozygous129777114
X107540136107540138GC5GENIChomozygous129777115
X107540140107540142GG5GENIChomozygous129777116
X107540143107540144GT5GENIChomozygous108411987
X107540146107540148GA5GENIChomozygous129777117
X107540154107540155G6GENIChomozygous129777118
X107540165107540166T9GENIChomozygous129777119
X107540172107540173TG10GENIChomozygous108308335
X107540127107540128AT4GENIChomozygous108452344
X107540156107540157GA7GENIChomozygous108308333