chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108636859486368595AT9GENIChomozygous116667508
108636864886368649CG12GENIChomozygous116667510
108636996186369962GA15GENIChomozygous116667512
108636997986369980GT5GENIChomozygous116667514
108637025986370260GC15GENIChomozygous116667516
108637029886370299GA17GENIChomozygous116667518
108637108886371089TC7GENIChomozygous116667520
108637596086375961CT13GENICheterozygous116667522
108637599386375994GT16GENIChomozygous116667524
108637641386376414CT8GENIChomozygous116667526
108637681686376817GA16GENIChomozygous116667528
108637696086376961CG9GENIChomozygous116667530
108637703386377034CT5GENIChomozygous116667532
108637790186377902AG24GENIChomozygous116667534
108637837186378372CT12GENIChomozygous116667536
108637929186379292AG14GENIChomozygous116667542
108638010086380101AG13GENIChomozygous116667544
108638209786382098GT11GENIChomozygous116667546
108638218586382186GA11GENIChomozygous116667548
108638400686384007GA7GENIChomozygous118005151
108638428286384283GA19GENIChomozygous126389145
108637062886370629TA11GENIChomozygous126389142
108638177986381780CA14GENIChomozygous126389143
108638514886385149AG7GENIChomozygous126389146
108638572786385728CG12GENIChomozygous126389147
108638648786386488GA18GENIChomozygous126389148
108638944386389444AG7GENIChomozygous126389149
108638990486389905CG6GENIChomozygous126389150
108639010486390105CT4GENIChomozygous126389151
108639106986391070TC4GENIChomozygous126389152
108639108286391083TC4GENIChomozygous126389153
108639122486391225TC12GENIChomozygous126389154
108639107686391077GA4GENIChomozygous126424817
108638505286385053AG10GENIChomozygous126424816