chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X127094670127094671GA9GENIChomozygous140702742
X127095791127095792TC8GENIChomozygous140702743
X127097654127097655T4GENIChomozygous140597182
X127102371127102372T7GENIChomozygous140597183
X127105770127105770TT15GENIChomozygous140597185
X127105864127105865AG15GENIChomozygous140702744
X127110928127110928AGTC11GENIChomozygous140597186
X127112978127112979AG13GENIChomozygous140702745
X127114132127114133AT4GENIChomozygous140702746
X127114338127114339CT5GENIChomozygous140702747
X127114447127114448AT8GENIChomozygous140702748
X127115029127115030CG9GENIChomozygous140702749
X127115143127115144TC9GENIChomozygous140702750
X127115696127115697AT11GENIChomozygous140702751
X127115749127115750GA15GENIChomozygous140702752
X127116439127116440AC6GENIChomozygous140702753
X127116887127116888TG7GENIChomozygous140702754
X127117147127117148CT13GENIChomozygous140702755
X127117604127117605CT12GENIChomozygous140702756
X127119989127119990CT10GENIChomozygous140702757
X127120669127120670AC16GENIChomozygous140702758
X127121056127121057TA6GENIChomozygous140702759
X127121643127121644TG8GENIChomozygous140702760
X127122368127122369CT14GENIChomozygous140702761
X127128479127128480GA18GENIChomozygous140702762
X127130399127130400AG12GENIChomozygous140702763
X127130455127130456AT8GENIChomozygous140702764
X127132623127132623T6GENIChomozygous140597187
X127133993127133994GT4GENIChomozygous140702765
X127138814127138815AG7GENIChomozygous140702766
X127139427127139428GA14GENIChomozygous140702767