chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117458900117458901C40GENIChomozygous128635832
8117460914117460915GT61GENICpossibly homozygous116671504
8117462354117462355CT47GENIChomozygous116671506
8117463142117463143AG40GENIChomozygous116671508
8117463763117463764CT34GENIChomozygous116671510
8117464369117464370AG16GENIChomozygous116671512
8117464395117464396CG24GENIChomozygous116671514
8117464601117464602TC38GENIChomozygous116671516
8117464876117464877GA48GENIChomozygous116671518
8117466249117466250AC52GENIChomozygous116671520
8117466513117466514TC43GENIChomozygous116671522
8117466898117466898GG23GENIChomozygous128635833
8117467475117467476TG25GENIChomozygous116671524
8117467476117467477TG25GENIChomozygous116671526
8117467952117467953AG29GENIChomozygous116671528
8117468441117468442GA35GENIChomozygous116671530
8117468564117468565GA16GENIChomozygous116671532
8117468864117468865CG21GENIChomozygous116671534
8117469362117469363TC47GENIChomozygous116671536
8117470014117470015TC58GENIChomozygous116671538
8117470387117470388GA54GENIChomozygous116671540
8117471283117471284TC57GENIChomozygous116671542
8117471357117471358AT48GENIChomozygous116671544
8117471931117471932TG55GENIChomozygous116671546
8117471948117471949GT45GENIChomozygous116671548
8117472015117472016TC38GENIChomozygous116671552
8117472671117472672G48GENIChomozygous128635834
8117473215117473216GA52GENIChomozygous116671554
8117473754117473754CCTCCCCAT12GENIChomozygous128635835
8117473789117473790AG18GENIChomozygous116671556
8117473918117473919AT25GENIChomozygous116671568
8117473986117473987CT32GENICpossibly homozygous116671574
8117474719117474721TC22GENICheterozygous128635836
8117475110117475111CA52GENIChomozygous116671590