chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1247110786247110787TA53GENIChomozygous108602475
1247113781247113782GA53GENICpossibly homozygous108602476
1247114110247114111GA14GENICheterozygous108602477
1247115396247115397GC35GENIChomozygous108602478
1247115987247115988TC31GENIChomozygous108602479
1247121986247121987GA25GENIChomozygous108602480
1247122296247122297CT29GENIChomozygous108602481
1247123104247123105TG44GENIChomozygous108602482
1247123243247123244TC30GENIChomozygous108602483
1247123385247123386GA37GENICpossibly homozygous108602484
1247128536247128537CT79GENICheterozygous108602485
1247128539247128540GC76GENICheterozygous108602486
1247129663247129664AG36GENIChomozygous108602487
1247133514247133515TC40GENIChomozygous108602488
1247134069247134070CT28GENIChomozygous108602489
1247134937247134938AG38GENIChomozygous108602490
1247135356247135357GA41GENIChomozygous108602491
1247136207247136208GC47GENIChomozygous108602492
1247138598247138599TC32GENIChomozygous108602493