chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1233991319233991320CT22GENIChomozygous61808711
1233991325233991326GT22GENIChomozygous61607963
1233991565233991566TC14GENIChomozygous61607964
1233992985233992986TC36GENIChomozygous61607965
1233994309233994310GA28GENIChomozygous61808712
1233995324233995325CT38GENIChomozygous61607967
1233995889233995890AT27GENIChomozygous61607968
1233997361233997362TTTG11GENICheterozygous62203785
1233997662233997663CG25GENIChomozygous61808713
1233998311233998312CCA23GENIChomozygous61607972
1233998599233998601TG--22GENIChomozygous61808714
1233998636233998637GT22GENIChomozygous61808715
1233998710233998711GA25GENIChomozygous61607974
1233999064233999065CT31GENIChomozygous61607975
1233999950233999955TGGAT-----30GENIChomozygous61607976
1234000509234000513AGTC----20GENIChomozygous61808716