chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1792191009219101GA48GENIChomozygous144180647
1792193739219374CT48GENIChomozygous144180648
1792210089221009GA56GENIChomozygous144180649
1792211729221173CG58GENIChomozygous144180650
1792218439221844CT42GENIChomozygous144180651
1792218759221876AG40GENIChomozygous144180652
1792219109221911TC35GENIChomozygous140051279
1792222229222223CT42GENIChomozygous144180653
1792228319222832TG22GENIChomozygous144180654
1792235699223570CG65GENIChomozygous144180655
1792239159223916TC51GENIChomozygous140051281
1792242659224266TC38GENIChomozygous144180656
1792250119225012TC60GENIChomozygous144180657
1792251029225103GA32GENICheterozygous155013656
1792251839225184CT43GENIChomozygous144180658
1792262929226293CG54GENIChomozygous144180659
1792265519226552CA53GENIChomozygous144180660
1792268279226828CT48GENIChomozygous144180661
1792274779227478TC48GENIChomozygous140051284
1792281089228109TC53GENIChomozygous140051285
1792282669228267AG56GENIChomozygous144180662
1792286849228685TC18GENIChomozygous144180663
1792299909229991TC50GENIChomozygous140051287
1792308149230815CT57GENIChomozygous140051288
1792313669231367AG65GENIChomozygous140051289
1792321799232180CT52GENIChomozygous144180664
1792332909233291TC60GENIChomozygous140051291
1792335279233528TA69GENIChomozygous140051292
1792336139233614CA65GENIChomozygous140051293
1792336709233671TC45GENIChomozygous140051294
1792337939233794AG42GENIChomozygous140051295
1792338349233835TC52GENIChomozygous140051297
1792286749228679TTTCT20GENIChomozygous144171789
1792213509221350A39GENIChomozygous144171786
1792238449223849CCAAA43GENIChomozygous144171787
1792257689225769C18GENIChomozygous144171788
1792318139231813TA40GENIChomozygous144171790
1792228229222823T22GENIChomozygous140008534
1792258539225855TG28GENIChomozygous140008535
1792318439231843A48GENIChomozygous140008537
1792320949232095T46GENIChomozygous140008538
1792251029225103G32GENICheterozygous403406297
1792261709226170A31GENICpossibly homozygous143626914