chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1792211229221123CT18GENIChomozygous140051278
1792219109221911TC19GENIChomozygous140051279
1792225679222568TG21GENIChomozygous140051280
1792239159223916TC14GENIChomozygous140051281
1792243289224329TA16GENIChomozygous140051282
1792250739225074GA9GENIChomozygous140051283
1792251029225103GA9GENICpossibly homozygous155013656
1792274779227478TC20GENIChomozygous140051284
1792281089228109TC15GENIChomozygous140051285
1792295529229553CA18GENIChomozygous140051286
1792299909229991TC20GENIChomozygous140051287
1792308149230815CT21GENIChomozygous140051288
1792313669231367AG21GENIChomozygous140051289
1792321649232165GA14GENIChomozygous140051290
1792332909233291TC14GENIChomozygous140051291
1792335279233528TA19GENIChomozygous140051292
1792336139233614CA15GENIChomozygous140051293
1792336709233671TC15GENIChomozygous140051294
1792337939233794AG14GENIChomozygous140051295
1792338049233805CT12GENIChomozygous140051296
1792338349233835TC12GENIChomozygous140051297
1792316379231637T8GENIChomozygous140008536
1792225649222567ATC21GENIChomozygous140008533
1792228229222823T18GENIChomozygous140008534
1792258539225855TG14GENIChomozygous140008535
1792318439231843A12GENIChomozygous140008537
1792320949232095T9GENIChomozygous140008538
1792251029225103G9GENICheterozygous403406297