chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1233991319233991320CT19GENIChomozygous61808711
1233991325233991326GT23GENIChomozygous61607963
1233991565233991566TC19GENIChomozygous61607964
1233992985233992986TC13GENIChomozygous61607965
1233994309233994310GA12GENIChomozygous61808712
1233995324233995325CT36GENIChomozygous61607967
1233995889233995890AT16GENIChomozygous61607968
1233997361233997362TTTG8GENICheterozygous62203785
1233997662233997663CG14GENIChomozygous61808713
1233998311233998312CCA21GENIChomozygous61607972
1233998599233998601TG--21GENIChomozygous61808714
1233998636233998637GT24GENIChomozygous61808715
1233998710233998711GA27GENIChomozygous61607974
1233999064233999065CT30GENIChomozygous61607975
1233999950233999955TGGAT-----15GENIChomozygous61607976
1234000509234000513AGTC----19GENIChomozygous61808716