chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4168204450168204451GA50GENIChomozygous112943432
4168207872168207874AC42GENICheterozygous128102460
4168210362168210363GT20GENICheterozygous112943448
4168210391168210392T22GENICheterozygous130752904
4168210406168210407CT25GENICheterozygous112943450
4168230035168230036TC47GENIChomozygous112943476
4168240034168240034GGAGGGAGGGAGGGAGGGAGGGAGGGAG6GENIChomozygous129905447
4168262086168262087AC41GENICheterozygous112943508
4168262086168262086C40GENICheterozygous133478828
4168265473168265474A42GENICheterozygous128102479
4168281428168281428C39GENIChomozygous128102483
4168284448168284449AT40GENIChomozygous112943551
4168291957168291957A37GENIChomozygous128102487
4168292028168292028G32GENIChomozygous128102488
4168301555168301555CGCACGCG23GENIChomozygous132060628
4168309774168309775AT8GENIChomozygous112943589
4168309863168309864G1GENIChomozygous132060629
4168313769168313770TC22GENIChomozygous112943601
4168314075168314076AG10GENICpossibly homozygous128140570
4168317020168317021AT25GENICpossibly homozygous130307406
4168317023168317025TT29GENIChomozygous128102501
4168323574168323575G16GENIChomozygous128102504
4168323578168323579T16GENIChomozygous128102505
4168323591168323592A14GENIChomozygous128102506
4168323595168323596A14GENIChomozygous128102507
4168323596168323597GT14GENIChomozygous119283012
4168281303168281304TG33GENICheterozygous134006099