chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123016108430161085AG47GENIChomozygous781792907
123016320930163210AC58GENICheterozygous781792908
123016448630164487AC53GENIChomozygous781792909
123016545830165459GT63GENIChomozygous781792910
123016588930165890GA57GENIChomozygous781792911
123016640430166405CT59GENIChomozygous781792912
123016644930166450CT82GENIChomozygous781792913
123016646430166465CA85GENIChomozygous781792914
123016744530167446AG62GENICpossibly homozygous781792915
123016824030168241CA49GENICpossibly homozygous781792916
123016945530169456CT55GENIChomozygous781792917
123017028730170288AG73GENIChomozygous781792918
123017121730171218TC50GENIChomozygous781792919
123017124330171244GA48GENIChomozygous781792920
123017162730171628GA45GENIChomozygous781792921
123017268830172689TG22GENICpossibly homozygous781792922
123017282930172830AC51GENIChomozygous781792923
123017305530173056CT52GENICheterozygous781792924
123017306530173066CT56GENICheterozygous781792925
123017307530173076CT53GENICheterozygous781792926
123017308830173089CT50GENICheterozygous781792927
123017463330174634CT57GENIChomozygous781792928
123017500530175006GA50GENIChomozygous781792929
123017509930175100CT49GENIChomozygous781792930
123017613030176131GA67GENICpossibly homozygous781792931
123017632230176323TG62GENIChomozygous781792932
123017709930177100TC46GENIChomozygous781792933
123017713930177140CT72GENIChomozygous781792934
123017720130177202TC69GENIChomozygous781792935
123017731830177319GA46GENIChomozygous781792936
123017745230177453GC61GENIChomozygous781792937
123017745430177455TA60GENICpossibly homozygous781792938
123017758330177584TC73GENICpossibly homozygous781792939