chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85774804457748045GGTTTTTGGTTTTTTT2GENIChomozygous53576187
85774810357748104CT17GENIChomozygous52981645
85774824957748250AAC34GENIChomozygous52656442
85774842957748430A-38GENIChomozygous52981646
85774848757748491TTTT----15GENIChomozygous52981647
85774965457749655TTA2GENIChomozygous52981648
85774994057749941AAT19GENIChomozygous52981649
85775040757750408TTC17GENIChomozygous52981650
85775046657750470CCAA----17GENIChomozygous53576189
85775264457752645TC46GENIChomozygous52656456
85775316057753161TTA6GENIChomozygous52981652
85775567557755676GGCCTTCCTTCCTTCCTTCCTTCCTT9GENIChomozygous53576190
85775588657755887CT10GENIChomozygous52656466
85775604657756047CT32GENIChomozygous52981653
85775776857757769CCAA7GENICheterozygous54094107
85775777357757774GGAA2GENIChomozygous53576191
85775793457757935AG9GENIChomozygous52656468
85775949857759499GGT12GENIChomozygous52981655
85776431957764320AG51GENICpossibly homozygous52656489