chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85774804457748045GGTTTTTGGTTTTTTT11GENIChomozygous53576187
85774810357748104CT16GENIChomozygous52981645
85774824957748250AAC19GENIChomozygous52656442
85774842957748430A-25GENIChomozygous52981646
85774848757748491TTTT----18GENIChomozygous52981647
85774965457749655TTA3GENIChomozygous52981648
85774994057749941AAT18GENIChomozygous52981649
85775040757750408TTC23GENIChomozygous52981650
85775046657750470CCAA----18GENIChomozygous53576189
85775264457752645TC22GENIChomozygous52656456
85775316057753161TTA18GENIChomozygous52981652
85775567557755676GGCCTTCCTTCCTTCCTTCCTTCCTT2GENIChomozygous53576190
85775588657755887CT43GENIChomozygous52656466
85775604657756047CT20GENIChomozygous52981653
85775777357757774GGA8GENICpossibly homozygous52981654
85775793457757935AG9GENICpossibly homozygous52656468
85775949857759499GGT28GENIChomozygous52981655
85776431957764320AG16GENIChomozygous52656489