chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77094633970946340TG11GENIChomozygous116190861
77094645170946452CT16GENIChomozygous116190863
77094683170946832TC8GENIChomozygous116190865
77094721970947220GA13GENIChomozygous116190867
77094731170947312CT17GENIChomozygous116190869
77094783970947840TC23GENIChomozygous116190871
77094868770948688CT36GENIChomozygous116190873
77094996070949961AG20GENIChomozygous116190875
77095022470950225TC14GENIChomozygous116190877
77095168170951682GA27GENIChomozygous116190879
77095267770952678CT31GENIChomozygous116190881
77095331570953316TC15GENIChomozygous116190883
77095359870953599AG23GENIChomozygous116190885
77095362170953622AG16GENIChomozygous116190887
77095390370953904AG17GENIChomozygous116190889
77095474470954745CT15GENICpossibly homozygous116190891
77095507170955072CT21GENIChomozygous116190893
77095509870955099TC23GENIChomozygous116190895
77095891070958911CG15GENIChomozygous116190903
77096007970960080AG27GENIChomozygous115709371
77096009470960095AG18GENIChomozygous116190905
77096061370960614TC19GENIChomozygous116190907
77096069470960695AG24GENIChomozygous116190909
77096199370961994AG22GENIChomozygous115709375
77096297670962977TC21GENIChomozygous115709377