chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77094633970946340TG31GENICpossibly homozygous116190861
77094645170946452CT22GENIChomozygous116190863
77094683170946832TC17GENIChomozygous116190865
77094721970947220GA51GENIChomozygous116190867
77094731170947312CT40GENIChomozygous116190869
77094783970947840TC46GENIChomozygous116190871
77094868770948688CT63GENICpossibly homozygous116190873
77094996070949961AG54GENIChomozygous116190875
77095022470950225TC47GENICpossibly homozygous116190877
77095132670951327CA68GENICpossibly homozygous116291623
77095168170951682GA51GENICpossibly homozygous116190879
77095267770952678CT63GENIChomozygous116190881
77095331570953316TC58GENIChomozygous116190883
77095359870953599AG51GENIChomozygous116190885
77095362170953622AG46GENIChomozygous116190887
77095390370953904AG53GENIChomozygous116190889
77095474470954745CT35GENICpossibly homozygous116190891
77095507170955072CT45GENIChomozygous116190893
77095509870955099TC45GENIChomozygous116190895
77095694570956946CT11GENICpossibly homozygous116190897
77095715870957159CT43GENICheterozygous116190899
77095717570957176TC40GENICheterozygous116391208
77095720670957207GC28GENIChomozygous115709370
77095784670957847AC17GENIChomozygous116190901
77095891070958911CG40GENIChomozygous116190903
77096007970960080AG52GENIChomozygous115709371
77096009470960095AG40GENIChomozygous116190905
77096061370960614TC69GENIChomozygous116190907
77096069470960695AG65GENIChomozygous116190909
77096127370961274TC13GENICpossibly homozygous115709372
77096134470961345TC12GENIChomozygous116291624
77096134870961349CT17GENICheterozygous116391209
77096138970961390AC33GENICheterozygous116256648
77096144970961450CA44GENICheterozygous116256649
77096199370961994AG40GENIChomozygous115709375
77096297670962977TC39GENIChomozygous115709377