chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108213131982131320G-8GENIChomozygous51516668
108213134682131347C-8GENIChomozygous51516669
108213362782133628A-10GENIChomozygous52068528
108213449582134496GT11GENIChomozygous51516690
108213769082137691C-2GENICheterozygous51516710
108213897882138979GT18GENIChomozygous51516720
108213898382138984CT18GENIChomozygous51516721
108213899882138999GT23GENIChomozygous51516722
108213900082139001AT23GENIChomozygous51516723
108213900782139008AT23GENIChomozygous51516724
108213901982139020AT23GENIChomozygous51516725
108213925882139259CG17GENIChomozygous51516729
108213926282139263AAG17GENIChomozygous51516730
108213926882139269A-19GENIChomozygous51516731
108214005982140061TT--8GENICheterozygous51717142
108214006082140061T-8GENICheterozygous51516732
108214458682144588CA--5GENIChomozygous51516752
108213463682134638TG--2GENIChomozygous52390724
108213896182138962GT15GENIChomozygous52390726
108214005882140059CCT8GENICheterozygous52461988
108214765382147654T-15INTERGENICheterozygous52461990
108214765282147654TT--15INTERGENICheterozygous52603075
108216039082160391TG13INTERGENIChomozygous51516792
108216039182160392TA13INTERGENIChomozygous51516793
108216039682160397C-13INTERGENIChomozygous51516794
108216039782160398CG13INTERGENIChomozygous52390728
108216161582161616G-24INTERGENICheterozygous51516802
108216182082161821GGACACCTCTGTCTCC8INTERGENICheterozygous51516803
108216443782164438CCT1INTERGENIChomozygous52444016
108217776782177768CCT2GENICheterozygous52390732
108218548182185482CCA22GENIChomozygous51516834