chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2055370275537028GT43GENIChomozygous109078348
2055374315537432GT34GENICpossibly homozygous109078350
2055376745537675CT51GENIChomozygous109078352
2055385705538571TC54GENIChomozygous109078356
2055386875538688AG37GENIChomozygous109078358
2055392155539216GA36GENIChomozygous109078360
2055401895540190GA22GENIChomozygous109078362
2055408935540894CT8GENIChomozygous109078364
2055444015544402TC33GENIChomozygous109078368
2055446605544661CT39GENIChomozygous109078370
2055447835544784CG27GENIChomozygous109078372
2055450675545068AC52GENIChomozygous109078374
2055456015545602CT13GENIChomozygous109078376
2055482565548257AG34GENICpossibly homozygous109078380
2055491435549144GA32GENIChomozygous109078382
2055491945549195CT30GENIChomozygous109078384
2055494005549401TC37GENIChomozygous109078386
2055494235549424TC39GENIChomozygous109078388
2055494735549474CT41GENIChomozygous109078390
2055495955549596CT37GENIChomozygous109078392
2055499785549979GA35GENIChomozygous109078394
2055499975549998GA31GENIChomozygous109078396
2055503555550356CA48GENIChomozygous109234119
2055503635550364GA41GENIChomozygous109078400
2055506745550675TC52GENIChomozygous109078402
2055516545551655CT50GENIChomozygous109078406
2055524705552471AG24GENIChomozygous109078410
2055526895552690GC34GENIChomozygous109078412
2055527715552772AG36GENIChomozygous109078414
2055535515553552GA23GENIChomozygous109078416
2055545585554559GA27GENIChomozygous109078418
2055546605554661GA34GENIChomozygous109078420
2055554905555491CA12GENIChomozygous109078422
2055575765557577CG23GENIChomozygous109078424
2055577345557735CT23GENIChomozygous109234120
2055582475558248AG37GENIChomozygous109078428
2055594455559446GA30GENIChomozygous109078430
2055600335560034CT24GENIChomozygous109078432
2055608675560868CT32GENIChomozygous109078434
2055619895561990AG29GENIChomozygous109078437
2055620065562007CT31GENIChomozygous109078439
2055629105562911GA39GENIChomozygous109078441
2055631865563187TC47GENIChomozygous109078443