chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77557237875572379TA17GENIChomozygous53979866
77557387675573878TC--30GENICheterozygous54658858
77557388975573890GGTC23GENICheterozygous53979872
77557388975573890GC35GENICheterozygous54658860
77557441675574419CCC---12GENICheterozygous53979876
77557441875574419C-12GENICheterozygous53979878
77557466575574666CT18GENIChomozygous53979880
77557466675574667AG17GENIChomozygous53979882
77557468275574683AG15GENIChomozygous53979884
77557681975576820CCT22GENIChomozygous54202590
77557805875578059A-13GENICheterozygous54202591
77557807775578078AC16GENICpossibly homozygous54202592
77557853975578540AG25GENICheterozygous53979908
77557859075578591TC34GENICheterozygous53979910
77557861275578613TC34GENICheterozygous54202594
77557861475578615AG33GENICheterozygous54202595
77557863975578640AG28GENICheterozygous53979912
77557997975579980GA15GENICheterozygous54202596
77558000475580006CA--12GENICheterozygous53979926
77558171775581718AAT10GENICheterozygous53979943
77558171875581719AT24GENIChomozygous53979945
77558171875581719AAAT18GENICheterozygous53979947
77558289475582896TG--14GENIChomozygous54202598
77558335375583354GGT11GENICheterozygous54202599