chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X106565731106565732AG8GENIChomozygous108411150
X106567095106567096GA10GENIChomozygous108411152
X106569854106569855CT4GENIChomozygous108411154
X106572436106572437AT19GENIChomozygous108411156
X106573279106573280CT7GENIChomozygous108411158
X106573420106573421AC6GENIChomozygous108411160
X106573724106573725GA6GENIChomozygous108411162
X106575485106575486CG5GENIChomozygous108411164
X106575712106575713TC10GENIChomozygous108411166
X106577633106577634GA7GENIChomozygous108411168
X106577931106577932AG5GENIChomozygous108411170
X106578015106578016GA10GENIChomozygous108411172
X106578224106578225CT9GENIChomozygous108411174
X106578590106578591TC8GENIChomozygous108411176
X106579733106579734TC7GENIChomozygous108411178
X106581198106581199AG2GENIChomozygous108411180
X106582353106582354GT8GENIChomozygous108411182
X106585447106585448GA3GENIChomozygous108411184
X106587303106587304TC7GENIChomozygous108411186
X106587315106587316CG14GENIChomozygous108411188