chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152250868622508687CT17GENICpossibly homozygous48255733
152250888822508889TG25GENIChomozygous49039878
152250889422508895GGA22GENIChomozygous49039880
152250957822509579CT15GENIChomozygous48255736
152250958222509583TC13GENIChomozygous48255737
152251031522510316AAAAAC11GENIChomozygous49039882
152251034022510344AGAG----6GENIChomozygous49039884
152251089222510893AG31GENIChomozygous48255739
152251133222511333AG20GENIChomozygous48255740
152251206622512067AG28GENIChomozygous48255741