chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
78356571683565717AT20GENIChomozygous886645815
78356603683566037TC15GENIChomozygous886645816
78356730683567307CT5GENIChomozygous886645817
78356883483568835TA5GENIChomozygous886645818
78356909183569092GA14GENIChomozygous886645819
78356927283569273AG16GENIChomozygous886645820
78356962683569627TA3GENICheterozygous886645821
78356998683569987GA13GENIChomozygous886645822
78357005383570054TG23GENIChomozygous886645823
78357084983570850CT10GENIChomozygous886645824
78357154283571543TG29GENIChomozygous886645825
78357241383572414GC18GENIChomozygous886645826
78357313583573136CA19GENICpossibly homozygous886645827
78357557383575574TC17GENIChomozygous886645828
78357592183575922GA20GENIChomozygous886645829
78357616983576170TG21GENIChomozygous886645830
78357676283576763AG9GENICheterozygous886645831
78357902083579021TC20GENIChomozygous886645832
78358005483580055AG31GENIChomozygous886645833
78358095083580951GA4GENIChomozygous886645834
78358096083580961CT5GENIChomozygous886645835
78358114783581148GA15GENIChomozygous886645836
78358150483581505GA20GENIChomozygous886645837
78358156183581562TG13GENIChomozygous886645838
78358222983582230GT17GENIChomozygous886645839