chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171091478310914784AG20GENIChomozygous110955606
171091505510915056AG19GENIChomozygous110955608
171091511210915113CT22GENIChomozygous110955610
171091514010915141AG19GENIChomozygous110955612
171091543010915431CG41GENIChomozygous110955614
171091548510915486CA34GENICpossibly homozygous119264135
171091558710915588GA24GENICheterozygous119264136
171091559210915593AG22GENICheterozygous119264137
171091570510915706AG20GENICheterozygous119264138
171091571110915712AG19GENICheterozygous111332330
171091576110915762AG23GENIChomozygous111332332
171091588610915887TG40GENIChomozygous110955616
171091602710916028CT30GENIChomozygous110955618
171091741010917411TC34GENIChomozygous110955620
171091753910917540GT19GENIChomozygous110955622
171091771410917715AC34GENIChomozygous110955624
171091800010918001TC29GENIChomozygous110955626
171091804210918043CT19GENIChomozygous110955628
171091804510918046GA21GENIChomozygous110955630
171091805210918053CT21GENIChomozygous110955632
171091806310918064GA21GENIChomozygous110955634
171091807810918079TC24GENIChomozygous110955636
171091816210918163AC29GENIChomozygous110955638
171091863010918631TC27GENIChomozygous110955640
171092005010920051GA38GENIChomozygous110955642
171092038010920381CT29GENIChomozygous110955644
171092088110920882AG35GENIChomozygous110955646
171092090410920905TC42GENIChomozygous110955648
171092117910921180GC39GENIChomozygous110955650
171092131610921317TA39GENIChomozygous110955652
171092167910921680TG40GENIChomozygous110955654
171092264910922650AG32GENIChomozygous110955656
171091581810915819TA30GENIChomozygous111231110
171092278410922785GC30GENIChomozygous110955658
171092377510923776CT21GENIChomozygous110955660
171092652010926521TG19GENICpossibly homozygous110955662
171092883510928836CT43GENIChomozygous110955664
171092935410929355CT28GENIChomozygous110955666
171092981410929815TG44GENIChomozygous110955668
171093109510931096TC21GENIChomozygous110955670