chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1233991319233991320CT10GENIChomozygous61808711
1233991325233991326GT8GENIChomozygous61607963
1233991565233991566TC11GENIChomozygous61607964
1233992985233992986TC11GENIChomozygous61607965
1233994309233994310GA9GENIChomozygous61808712
1233995324233995325CT25GENIChomozygous61607967
1233995889233995890AT13GENIChomozygous61607968
1233997361233997362TTTG5GENICheterozygous62203785
1233997662233997663CG23GENIChomozygous61808713
1233998311233998312CCA17GENIChomozygous61607972
1233998599233998601TG--11GENIChomozygous61808714
1233998636233998637GT14GENIChomozygous61808715
1233998710233998711GA17GENIChomozygous61607974
1233999064233999065CT22GENIChomozygous61607975
1233999950233999955TGGAT-----17GENIChomozygous61607976
1234000509234000513AGTC----13GENIChomozygous61808716