chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83676092036760921TC29GENIChomozygous116456978
83676103736761038GA63GENIChomozygous116456979
83676117736761178GC68GENICpossibly homozygous116456980
83676148036761481CG71GENIChomozygous116456981
83676165036761651TC59GENIChomozygous116456982
83676168036761681CA56GENIChomozygous116456983
83676184836761849AG62GENIChomozygous116456984
83676207836762079CT76GENIChomozygous116456985
83676214736762148GT81GENICpossibly homozygous116456986
83676223736762238TA57GENIChomozygous116456987
83676240236762403AG59GENIChomozygous116456988
83676258936762590AC74GENIChomozygous116456989
83676275136762752TA93GENIChomozygous116456990
83676322536763226TC64GENIChomozygous116456991
83676415436764155TC62GENIChomozygous116456992
83676428236764283CT52GENIChomozygous116456993
83676449336764494GA75GENIChomozygous116456994
83676450636764507TC74GENICpossibly homozygous116456995
83676455236764553CT73GENIChomozygous116456996
83676457836764579AG73GENICpossibly homozygous116456997
83676481636764817TC89GENICpossibly homozygous116456998
83676483436764835GC85GENIChomozygous116456999
83676491636764917AG53GENIChomozygous116457000
83676532836765329GA75GENICpossibly homozygous116457001
83676544736765448GA72GENIChomozygous116457002
83676613336766134AG82GENIChomozygous116457003
83676686736766868GA61GENIChomozygous116457004
83676711736767118AG64GENIChomozygous116457005
83676762036767621CT64GENIChomozygous116457006
83676807436768075AG47GENIChomozygous116457007
83676908836769089CT47GENIChomozygous116457008