chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1247110786247110787TA34GENIChomozygous108602475
1247111529247111530GA25GENIChomozygous108775374
1247115137247115138GA29GENIChomozygous108775375
1247115987247115988TC36GENIChomozygous108602479
1247116075247116076TC26GENIChomozygous108775376
1247121986247121987GA3GENIChomozygous108602480
1247123104247123105TG15GENIChomozygous108602482
1247123243247123244TC26GENIChomozygous108602483
1247124524247124525GA13GENIChomozygous108775377
1247125564247125565CG32GENIChomozygous108775378
1247126220247126221AG31GENIChomozygous108775379
1247129847247129848CT27GENIChomozygous108775382
1247132864247132865GA38GENIChomozygous108775384
1247133514247133515TC34GENIChomozygous108602488
1247133966247133967TG30GENIChomozygous108775385
1247134069247134070CT32GENIChomozygous108602489
1247134553247134554CA8GENIChomozygous108775386
1247136207247136208GC17GENIChomozygous108602492
1247138284247138285AG23GENIChomozygous108775387