chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X122726773122726774CG4GENICheterozygous120731603
X122728408122728408TTT11GENIChomozygous129785755
X122729841122729842AC17GENIChomozygous108423556
X122749403122749404TC5GENIChomozygous108423558
X122754042122754042C7GENIChomozygous129785760
X122777744122777745C2GENIChomozygous129785776
X122777758122777759T3GENIChomozygous129785777
X122777783122777784T3GENIChomozygous129785778
X122777796122777797T3GENIChomozygous129785779
X122777804122777805A3GENIChomozygous129785780
X122777816122777817GC3GENIChomozygous119951025
X122777820122777820C3GENIChomozygous129785781
X122777827122777828C3GENIChomozygous129785782
X122777854122777855TA3GENIChomozygous120731647
X122777861122777862GC3GENIChomozygous108599391
X122777901122777902GA6GENIChomozygous108323150
X122777931122777932C6GENIChomozygous129785783
X122777946122777947T6GENIChomozygous129785784
X122777959122777959A8GENIChomozygous129785785
X122777970122777971TA8GENIChomozygous108323152
X122778018122778019A9GENIChomozygous129785786
X122778033122778034T8GENIChomozygous129785787
X122783800122783801A12GENIChomozygous129785791
X122770268122770268TGTATGGGCCACATG4GENIChomozygous130502002
X122777853122777854AT3GENIChomozygous108688498