chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7106556301106556302GA28GENIChomozygous138174089
7106556445106556446GA20GENICpossibly homozygous138174090
7106557045106557046GA17GENIChomozygous138174091
7106557088106557089GC17GENIChomozygous138174092
7106557117106557118AG18GENIChomozygous138174093
7106557207106557208TC20GENIChomozygous138174094
7106557650106557651GA25GENIChomozygous138174095
7106557730106557730TG25GENIChomozygous137972510
7106558179106558180GA29GENIChomozygous138174096
7106559345106559346AG12GENIChomozygous138174097