chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2040221984022199CA15GENIChomozygous63662059
2040244154024416CT5GENIChomozygous63662060
2040252374025238AG12GENIChomozygous63335520
2040252934025294GA9GENIChomozygous63662061
2040256344025635CT16GENIChomozygous63335522
2040258244025825CT6GENIChomozygous63662062
2040259124025913GA14GENIChomozygous63662063
2040269234026924AC20GENIChomozygous63563653
2040277844027785GA11GENIChomozygous63662064
2040278394027840CT14GENIChomozygous63563655
2040279374027938TC7GENIChomozygous63335524
2040281264028127AT14GENIChomozygous63335527
2040283234028324CT9GENIChomozygous63335528
2040287154028716TC6GENIChomozygous63563657
2040297814029782GA5GENIChomozygous63662065
2040310624031063CT10GENIChomozygous63662066
2040310994031100CA13GENIChomozygous63335530
2040314014031402AG14GENIChomozygous63640932
2040314044031405GA14GENIChomozygous63335532
2040316134031614GA15GENIChomozygous63640933
2040316664031667CT12GENICpossibly homozygous63335533
2040317054031706CA19GENIChomozygous63335534
2040317524031753AT22GENIChomozygous63640934
2040318314031832CT14GENIChomozygous63335535
2040320374032038GA14GENIChomozygous63335537
2040322614032262CT10GENIChomozygous63662067
2040323734032374GA12GENIChomozygous63662068
2040328724032873GA17GENIChomozygous63640935
2040331654033166GT9GENIChomozygous63662069
2040332264033227GA18GENIChomozygous63640936