chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77094633970946340TG18GENIChomozygous116190861
77094645170946452CT14GENIChomozygous116190863
77094659470946594G13GENIChomozygous131019492
77094683170946832TC27GENIChomozygous116190865
77094698970946989A16GENIChomozygous131019493
77094721970947220GA17GENIChomozygous116190867
77094731170947312CT12GENIChomozygous116190869
77094753070947549TGGGAGTAAGAACTCGGAG25GENIChomozygous131019494
77094783970947840TC17GENIChomozygous116190871
77094868770948688CT21GENIChomozygous116190873
77094996070949961AG21GENIChomozygous116190875
77095022470950225TC16GENIChomozygous116190877
77095168170951682GA22GENIChomozygous116190879
77095244370952443TTTTG10GENIChomozygous131019495
77095267770952678CT22GENIChomozygous116190881
77095331570953316TC18GENIChomozygous116190883
77095359870953599AG8GENIChomozygous116190885
77095362170953622AG7GENIChomozygous116190887
77095390370953904AG18GENIChomozygous116190889
77095474470954745CT17GENIChomozygous116190891
77095507170955072CT12GENIChomozygous116190893
77095509870955099TC16GENIChomozygous116190895
77095576270955762ACA15GENIChomozygous131019496
77095686370956863G14GENIChomozygous131019497
77095694570956946CT7GENIChomozygous116190897
77095720670957207GC12GENIChomozygous115709370
77095792870957929C4GENIChomozygous128478085
77095793370957933T4GENIChomozygous128478086
77095799170957991G15GENIChomozygous128478088
77095804170958041G25GENIChomozygous128478089
77095891070958911CG17GENIChomozygous116190903
77096007970960080AG19GENIChomozygous115709371
77096009470960095AG20GENIChomozygous116190905
77096061370960614TC22GENIChomozygous116190907
77096069470960695AG14GENIChomozygous116190909
77096199370961994AG8GENIChomozygous115709375
77096297670962977TC13GENIChomozygous115709377