chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153440217153440218TC34GENIChomozygous112889639
4153440872153440873AG27GENIChomozygous112889640
4153441741153441742GA19GENIChomozygous112889641
4153442622153442623AG29GENIChomozygous112889642
4153443106153443107GA35GENIChomozygous112889643
4153444721153444722AG35GENIChomozygous112889644
4153444950153444951AG47GENIChomozygous112889645
4153446959153446960AG15GENIChomozygous112889646
4153447180153447181TG30GENIChomozygous112889647
4153447543153447544GT30GENIChomozygous112889648
4153447546153447547GA30GENIChomozygous112889649
4153449027153449028CT42GENIChomozygous112889650
4153449095153449096GA52GENIChomozygous112889651
4153449504153449505AC35GENIChomozygous112889652
4153449692153449693CT25GENIChomozygous112889653
4153449728153449729TC28GENIChomozygous112889654
4153450520153450521AG33GENIChomozygous112889655
4153450923153450924CT28GENIChomozygous112889656
4153451325153451326AG26GENIChomozygous112889657
4153452743153452744TC24GENIChomozygous112889658
4153455143153455144TA14GENIChomozygous112889659
4153455403153455404CG30GENIChomozygous112889660
4153455505153455506AG5GENIChomozygous112889663
4153457169153457170CT24GENIChomozygous112889664
4153457255153457256AC33GENIChomozygous112889665
4153458242153458243AT17GENIChomozygous112889666
4153458499153458500CA19GENIChomozygous113061231
4153458962153458963CT24GENIChomozygous112889667
4153459248153459249TG34GENIChomozygous112889668
4153459315153459316GA44GENIChomozygous112889669
4153460591153460592TC31GENIChomozygous112889670
4153460638153460639CT29GENIChomozygous112889671
4153460794153460795AG31GENIChomozygous112889672
4153461194153461195CT27GENIChomozygous112889673
4153462198153462199GA29GENIChomozygous112889675
4153463074153463075TA27GENIChomozygous112889676
4153463545153463546AG9GENIChomozygous112889677
4153464122153464123AG23GENIChomozygous112889678
4153465242153465243CT16GENIChomozygous112889679