chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87064097470640975AG33GENIChomozygous142078381
87064154170641541GTG20GENIChomozygous142025547
87064222870642229GA21GENIChomozygous142078382
87064387670643877AG20GENIChomozygous142078384
87064394570643946CT27GENIChomozygous142078385
87064455070644551AC24GENIChomozygous142078386
87064691570646917TC8GENIChomozygous142025548
87064921670649217GA22GENIChomozygous142078387
87064923170649232AG24GENIChomozygous142078388
87064952070649521TC30GENIChomozygous142078389
87064989770649897T30GENIChomozygous142025549
87065003270650033GA26GENIChomozygous142078390
87065227770652278CG32GENIChomozygous142078391
87065269970652699T13GENICpossibly homozygous142025550
87065295470652955AG24GENIChomozygous142078392
87065328670653389CAGGTAATTTTCTGAGAGTCCTTTTTTAAAAAAAAGTTCCTTGTATTTAAATGTCAGTTTTATGTGTCACAAGTCCTGAGGGTATTGTTTGTGTTTTTGTCCC57GENICheterozygous148528041
87065802870658029GA23GENIChomozygous142078395
87065541370655414AG32GENIChomozygous142078393
87065632970656330TC22GENIChomozygous142078394
87065713870657139GA43GENICheterozygous148531767
87065834870658349CT26GENIChomozygous142078396
87065920870659209TC34GENIChomozygous142078397
87066104870661049CT27GENIChomozygous142078398
87066112170661122AG14GENIChomozygous142078399