chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18362687383626874GA25GENIChomozygous109304331
18362710783627108TC16GENIChomozygous109304333
18362798083627981AG30GENIChomozygous108879582
18362829783628298AG22GENIChomozygous108879584
18362837383628374TC23GENIChomozygous109304335
18362839083628391CT27GENIChomozygous109304337
18362862883628629CT25GENICpossibly homozygous108879585
18362908083629081GA25GENIChomozygous109304339
18362970383629704GA21GENIChomozygous109304341
18363136183631362AG32GENIChomozygous109304343
18363176983631770AC39GENIChomozygous109304345
18363219383632194CA31GENIChomozygous109304347
18363348483633485GT18GENICpossibly homozygous109304349
18363408583634086TC25GENIChomozygous109304351
18363469983634700AG25GENIChomozygous108879589
18363474383634744CT28GENIChomozygous108879590
18363508183635082CT16GENIChomozygous109304353
18363516683635167AG19GENIChomozygous108879591
18363591183635912CA20GENIChomozygous109304355
18363611883636119TC35GENIChomozygous109304357
18363672583636726GA24GENIChomozygous109304359
18363723983637240TC31GENIChomozygous109304361
18363774483637745TC38GENIChomozygous108879593
18363779183637792CT27GENIChomozygous109304363