chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2039956323995633GA53INTERGENIChomozygous45374463
2039957743995775AG53INTERGENIChomozygous45374464
2039963743996375GA51GENIChomozygous45374465
2039964713996472TG48GENIChomozygous45374466
2039966473996648CT45GENIChomozygous45374467
2039966513996652GA42GENIChomozygous45374468
2039971243997130GTGTGT------3GENICheterozygous45374469
2039978713997874GGA---17GENIChomozygous45374470
2039978723997874GA--17GENIChomozygous45374471
2039978733997874A-17GENIChomozygous45374472
2039978733997874AAG14GENICheterozygous45374473
2039980013998002TTA27GENICheterozygous45374474
2039987603998761AG46GENIChomozygous45374475
2040013684001369AG71GENIChomozygous45374476
2040018874001888A-30GENIChomozygous45374477
2040025324002533AG49GENICpossibly homozygous45374478
2040026384002639TA53GENIChomozygous45374479
2040030864003087CT22GENICheterozygous45374480
2040034984003499AAAG33GENICpossibly homozygous45374481
2040035264003527CCAG47GENICheterozygous45374482
2040035384003539CCAG44GENICheterozygous45374483
2040035544003555GC59GENICheterozygous45374484
2040041354004136TC57GENIChomozygous45374485
2040044274004428G-43GENIChomozygous45374486
2040045894004590GA37GENIChomozygous45374487
2040047554004756TG43GENICpossibly homozygous45374488
2040047564004757CA42GENIChomozygous45374489
2040047634004764CT40GENICpossibly homozygous45374490
2040052844005285GA38GENIChomozygous45374491
2040055694005579ACACACACAC----------2GENICheterozygous45374492
2040055774005579AC--2GENICheterozygous45374493
2040062174006218AG38GENIChomozygous45374494
2040064404006441AG36GENIChomozygous45374495
2040065124006515AAA---1GENIChomozygous45374496
2040065494006550GA26GENICheterozygous45374497
2040076284007629AC29GENIChomozygous45374498
2040082944008295CT37GENIChomozygous45374499
2040093984009399G-37GENIChomozygous45374500