chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144264533144264534GA14GENIChomozygous976167942
7144265280144265281CT28GENIChomozygous976167943
7144265440144265441GA33GENIChomozygous976167944
7144265488144265489AG30GENIChomozygous976167945
7144265682144265683AG28GENIChomozygous976167946
7144265916144265917TC24GENICpossibly homozygous976167947
7144266105144266106TC21GENIChomozygous976167948
7144266678144266679GA17GENICpossibly homozygous976167949
7144266911144266912AT15GENIChomozygous976167950
7144267423144267424AG11GENIChomozygous976167951
7144267802144267803GA26GENIChomozygous976167952
7144267818144267819CT25GENIChomozygous976167953
7144269102144269103CT34GENIChomozygous976167954
7144270498144270499AG24GENIChomozygous976167955
7144270615144270616TC18GENIChomozygous976167956
7144271284144271285CT31GENIChomozygous976167957
7144271376144271377TC23GENIChomozygous976167958
7144271487144271488AG23GENIChomozygous976167959