chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75385907453859075GC9GENIChomozygous53926026
75385989853859899GA9GENIChomozygous53926027
75386039953860400CT1GENIChomozygous53926028
75386064653860647GGTGTC7GENIChomozygous55024476
75386100953861010CT10GENIChomozygous53926030
75386208253862084AC--4GENICheterozygous53926032
75386790453867905G-9GENIChomozygous53926033
75386844453868445GA6GENIChomozygous53926034
75386979353869795AA--6GENIChomozygous53926041
75387005153870055CGTT----3GENIChomozygous55141663
75387031453870315CG7GENIChomozygous53926045
75387109753871098GA8GENIChomozygous53926046
75387125153871252GA16GENIChomozygous53926047
75387134553871346TA9GENIChomozygous53926048
75387145353871454C-2GENICheterozygous53926049
75387175953871760GA4GENIChomozygous53926050
75387309153873092AACC7GENICpossibly homozygous53926053
75386045053860451CT1GENIChomozygous55355055
75387285253872858GAGAGA------1GENIChomozygous55355057
75386202453862025C-4GENICheterozygous54902712
75387309153873092AAAAC7GENICheterozygous54902714
75386980253869803AC6GENIChomozygous55310955
75387308153873082CA6GENIChomozygous54195748
75387308753873088CA7GENIChomozygous54195749
75387313153873132GA10GENIChomozygous53926054
75387677953876780CT3GENIChomozygous53926055
75387721353877214CCT10GENICpossibly homozygous53926056
75387732153877322CT3GENIChomozygous53926057
75387754453877545TC7GENIChomozygous53926058
75387761853877619AC7GENIChomozygous53926059
75387852253878523AC5GENIChomozygous53926060
75387925753879258TC5GENIChomozygous53926061
75387926053879261T-6GENIChomozygous55310964
75387975753879758AG2GENIChomozygous53926063
75388003053880031AC9GENIChomozygous53926064
75388382953883830AAT5GENIChomozygous53926065
75388416253884163A-4GENIChomozygous53926066
75388439453884395GA7GENIChomozygous53926067
75388713253887133CT8GENIChomozygous53926068
75388735253887368ACACACACACACACAC----------------3GENIChomozygous55355059
75388758453887585C-5GENICheterozygous53926070
75387688553876886CT6GENIChomozygous55862314