chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1670355267035527AG17GENIChomozygous111712256
1670357677035770ACT20GENIChomozygous129330400
1670410987041099AT16GENIChomozygous111712258
1670505517050552CT14GENICheterozygous119141635
1670387497038750AG19GENIChomozygous112102801
1670505297050530CT14GENICheterozygous119141633
1670504217050422CT17GENICheterozygous119093963
1670508857050886TC18GENICheterozygous132427928
1670511967051199TCA17GENIChomozygous132741390
1670515517051552CA16GENICpossibly homozygous119190787
1670531237053124AG21GENICheterozygous119141637
1670552107055211CT13GENIChomozygous119093967
1670552157055216TC15GENIChomozygous119093968
1670560727056073CT13GENIChomozygous112102803
1670567277056728TG18GENIChomozygous112102805
1670567577056758A17GENIChomozygous132204374
1670575717057572TA18GENIChomozygous111712268
1670586917058692AT16GENIChomozygous111712270
1670588077058811AGAC14GENIChomozygous132741391
1670593717059372CT20GENIChomozygous111712272
1670603417060342AT16GENIChomozygous111712274
1670603627060363G13GENIChomozygous129330404
1670603647060367TAG13GENIChomozygous129330405
1670604637060463T12GENIChomozygous129330406
1670621217062122CT15GENIChomozygous111712278
1670631977063197ACAGAGAGAA10GENIChomozygous129330407
1670638937063894GA10GENIChomozygous112102807
1670639727063973TC14GENIChomozygous111712283
1670650177065018AG19GENIChomozygous112433798
1670667867066787CT16GENIChomozygous111712285
1670693147069315CT17GENIChomozygous112102809
1670711237071124TC23GENIChomozygous119190790
1670727007072701CT13GENIChomozygous112102811
1670757347075735GA20GENIChomozygous112102813
1670791057079106GA18GENIChomozygous111712289
1670796787079679GT23GENIChomozygous111712291
1670798927079898AATTTT20GENIChomozygous129330412
1670799797079979ACTCTG20GENIChomozygous129330413
1670568537056858GTACT18GENIChomozygous131171802
1670565597056560CG21GENIChomozygous111927500