chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85151354951513550TA7GENIChomozygous52973768
85151373851513741CTG---4GENIChomozygous53318682
85151580451515805T-2GENIChomozygous52973775
85151592851515929CT20GENIChomozygous53318683
85151645951516460GA13GENICheterozygous52973780
85151713951517140CT13GENICpossibly homozygous53318684
85151759151517592AC29GENIChomozygous52973783
85151774151517742TG17GENIChomozygous53318685
85152079251520793GGCACT8GENIChomozygous53318686
85152138151521382CA6GENIChomozygous53117480
85152173451521735GT15GENICpossibly homozygous52973797
85152208751522088TC1GENIChomozygous52973799
85152646951526470GC13GENICheterozygous52973817
85152727951527283AAAA----1GENIChomozygous52973825
85152737051527371TC12GENIChomozygous53117481
85152769651527697AG19GENIChomozygous52973827
85152791051527914TGGA----6GENIChomozygous53117483
85152794751527948AG20GENIChomozygous52973833
85152827651528277GT2GENICheterozygous53117485
85152923951529240GA19GENIChomozygous53117487
85152972451529725A-1GENIChomozygous52626460
85152103851521039GGAGGAGGGGAAAAGT2GENIChomozygous52626454