chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887405140887406GC16GENIChomozygous975528907
4140887526140887527AG17GENIChomozygous975528908
4140892114140892115TA13GENIChomozygous975528909
4140894149140894150GA25GENIChomozygous975528910
4140894483140894484TC17GENIChomozygous975528911
4140894658140894659GC14GENIChomozygous975528912
4140896988140896989GA21GENIChomozygous975528913
4140899328140899329GA29GENIChomozygous975528914
4140901019140901020TC8GENIChomozygous975528915
4140902715140902716TC21GENIChomozygous975528916
4140902957140902958AG18GENIChomozygous975528917
4140903807140903808CT23GENIChomozygous975528918
4140906395140906396AG26GENIChomozygous975528919
4140908274140908275TG18GENIChomozygous975528920
4140908994140908995GC26GENIChomozygous975528921
4140909042140909043GA30GENIChomozygous975528922
4140909059140909060CA28GENIChomozygous975528923
4140909109140909110GA30GENIChomozygous975528924
4140909129140909130CT23GENIChomozygous975528925
4140909170140909171GA26GENIChomozygous975528926
4140909196140909197CT27GENIChomozygous975528927
4140909244140909245GT32GENIChomozygous975528928
4140909248140909249TA30GENIChomozygous975528929
4140909269140909270GA28GENIChomozygous975528930
4140909286140909287GC28GENIChomozygous975528931
4140913522140913523CT4GENIChomozygous975528932
4140916630140916631TG36GENIChomozygous975528933
4140916631140916632CA37GENIChomozygous975528934
4140916937140916938GA24GENIChomozygous975528935