chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4168204450168204451GA60GENIChomozygous112943432
4168210391168210392T23GENICheterozygous130752904
4168210406168210407CT26GENICheterozygous112943450
4168230035168230036TC55GENIChomozygous112943476
4168240034168240034GGAGGGAGGGAGGGAGGGAGGGAGGGAG6GENIChomozygous129905447
4168262086168262087AC41GENIChomozygous112943508
4168262632168262633A20GENICheterozygous132060627
4168265473168265474A47GENICheterozygous128102479
4168281428168281428C47GENIChomozygous128102483
4168284448168284449AT54GENIChomozygous112943551
4168291957168291957A28GENIChomozygous128102487
4168292028168292028G35GENIChomozygous128102488
4168301555168301555CGCACGCG33GENIChomozygous132060628
4168309774168309775AT5GENIChomozygous112943589
4168309863168309864G1GENIChomozygous132060629
4168313769168313770TC40GENIChomozygous112943601
4168314075168314076AG6GENIChomozygous128140570
4168317020168317021AT23GENICheterozygous130307406
4168317020168317020T23GENICheterozygous133395938
4168317023168317025TT26GENICpossibly homozygous128102501
4168323574168323575G29GENIChomozygous128102504
4168323578168323579T31GENIChomozygous128102505
4168323591168323592A30GENIChomozygous128102506
4168323595168323596A30GENIChomozygous128102507
4168323596168323597GT30GENIChomozygous119283012