chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122526669325266694GA62GENICheterozygous118301619
122526732725267328AG71GENIChomozygous115290078
122526735325267354GA74GENIChomozygous115369539
122526739525267396TC57GENIChomozygous115290080
122526745525267456CT44GENIChomozygous115290082
122526818125268182TC57GENIChomozygous115290084
122526825025268251CG63GENIChomozygous115290086
122526894425268945CT40GENICheterozygous115510253
122526950325269504GA35GENICheterozygous118301620
122526978725269788CT45GENIChomozygous115369541
122526985425269855AG46GENIChomozygous115290090
122527081625270817GA56GENICpossibly homozygous115290092
122527090425270905TC53GENIChomozygous115290094
122527099125270992TG60GENIChomozygous115290096
122527102325271024GA69GENIChomozygous115290098
122527175425271755TG40GENIChomozygous115290102
122527214525272146TC48GENIChomozygous115290104
122527259225272593TC32GENICpossibly homozygous115369543
122527261125272612CT39GENICpossibly homozygous115369545
122527274125272742CT55GENIChomozygous115290106
122527344325273444GA37GENIChomozygous118262502
122526953225269533GA33GENICpossibly homozygous118262500
122527116725271168CT64GENIChomozygous115598984
122527400625274007TC65GENIChomozygous115290108
122527414925274150AC53GENIChomozygous115369547
122527444025274441GA44GENIChomozygous115369549
122527500525275006TC49GENIChomozygous118301621
122528564225285643TG26GENIChomozygous118262504
122532360025323601CT35GENIChomozygous118301622
122533952225339523AG18GENICheterozygous118301623
122534139025341391AG38GENICpossibly homozygous118301624
122535991025359911GA43GENIChomozygous118301625
122536931325369314TG20GENICpossibly homozygous118301626
122537005225370053AG39GENIChomozygous118301627
122537031125370312CT65GENIChomozygous115598986
122537059225370593GT75GENIChomozygous115598988