chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83676092036760921TC76GENIChomozygous116456978
83676103736761038GA82GENIChomozygous116456979
83676117736761178GC63GENIChomozygous116456980
83676148036761481CG68GENIChomozygous116456981
83676165036761651TC64GENIChomozygous116456982
83676168036761681CA78GENIChomozygous116456983
83676184836761849AG68GENIChomozygous116456984
83676207836762079CT65GENIChomozygous116456985
83676214736762148GT71GENIChomozygous116456986
83676223736762238TA53GENIChomozygous116456987
83676240236762403AG69GENIChomozygous116456988
83676258936762590AC57GENIChomozygous116456989
83676275136762752TA57GENICpossibly homozygous116456990
83676303536763035T43GENIChomozygous128582694
83676318936763190A58GENIChomozygous128582695
83676189736761897GGAG58GENIChomozygous128582692
83676292536762928CTT52GENIChomozygous128582693
83676322536763226TC61GENIChomozygous116456991
83676415436764155TC63GENIChomozygous116456992
83676428236764283CT51GENIChomozygous116456993
83676449336764494GA55GENIChomozygous116456994
83676450636764507TC58GENIChomozygous116456995
83676455236764553CT55GENIChomozygous116456996
83676457836764579AG56GENIChomozygous116456997
83676481636764817TC72GENIChomozygous116456998
83676483436764835GC72GENIChomozygous116456999
83676491636764917AG67GENIChomozygous116457000
83676532836765329GA53GENIChomozygous116457001
83676544736765448GA60GENIChomozygous116457002
83676613336766134AG84GENIChomozygous116457003
83676679336766817CTGGAACTTGTCCTCCTGTCTCTT39GENIChomozygous128582696
83676686736766868GA42GENIChomozygous116457004
83676711736767118AG47GENIChomozygous116457005
83676762036767621CT76GENIChomozygous116457006
83676807436768075AG59GENIChomozygous116457007
83676908836769089CT65GENIChomozygous116457008