chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87064097470640975AG51GENIChomozygous142078381
87064154170641541GTG56GENIChomozygous142025547
87064222870642229GA63GENIChomozygous142078382
87064387670643877AG51GENIChomozygous142078384
87064394570643946CT55GENIChomozygous142078385
87064455070644551AC62GENIChomozygous142078386
87064691570646917TC6GENIChomozygous142025548
87064921670649217GA48GENIChomozygous142078387
87064923170649232AG51GENIChomozygous142078388
87064952070649521TC43GENIChomozygous142078389
87064989770649897T44GENIChomozygous142025549
87065003270650033GA41GENIChomozygous142078390
87065227770652278CG49GENIChomozygous142078391
87065269970652699T48GENICpossibly homozygous142025550
87065295470652955AG43GENIChomozygous142078392
87065541370655414AG58GENIChomozygous142078393
87064998570649986GA42GENIChomozygous147273327
87065632970656330TC62GENIChomozygous142078394
87065834870658349CT43GENIChomozygous142078396
87065920870659209TC52GENIChomozygous142078397
87066104870661049CT37GENIChomozygous142078398
87066112170661122AG29GENIChomozygous142078399