chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153440217153440218TC24GENIChomozygous112889639
4153440872153440873AG18GENIChomozygous112889640
4153441741153441742GA19GENIChomozygous112889641
4153442622153442623AG21GENIChomozygous112889642
4153443106153443107GA19GENIChomozygous112889643
4153444721153444722AG12GENIChomozygous112889644
4153444950153444951AG20GENIChomozygous112889645
4153446959153446960AG21GENIChomozygous112889646
4153447180153447181TG18GENIChomozygous112889647
4153447543153447544GT20GENIChomozygous112889648
4153447546153447547GA21GENIChomozygous112889649
4153449504153449505AC22GENIChomozygous112889652
4153449692153449693CT18GENIChomozygous112889653
4153449728153449729TC10GENIChomozygous112889654
4153450230153450231AC13GENICheterozygous119556615
4153450520153450521AG17GENIChomozygous112889655
4153450923153450924CT13GENIChomozygous112889656
4153451325153451326AG10GENIChomozygous112889657
4153452743153452744TC15GENIChomozygous112889658
4153455403153455404CG13GENIChomozygous112889660
4153455415153455416AT12GENIChomozygous112889661
4153455463153455464GT9GENIChomozygous112889662
4153457169153457170CT14GENIChomozygous112889664
4153457255153457256AC32GENIChomozygous112889665
4153458242153458243AT20GENIChomozygous112889666
4153458499153458500CA13GENIChomozygous113061231
4153458962153458963CT18GENIChomozygous112889667
4153459248153459249TG18GENIChomozygous112889668
4153459315153459316GA23GENIChomozygous112889669
4153460591153460592TC23GENIChomozygous112889670
4153460638153460639CT35GENICpossibly homozygous112889671
4153460794153460795AG17GENIChomozygous112889672
4153461194153461195CT24GENIChomozygous112889673
4153463074153463075TA12GENIChomozygous112889676
4153463545153463546AG6GENICheterozygous112889677
4153464122153464123AG17GENICpossibly homozygous112889678
4153465242153465243CT6GENIChomozygous112889679