chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143184329143184330GT23GENIChomozygous57506943
4143185628143185629C-20GENIChomozygous58082926
4143186668143186669TC25GENIChomozygous56961804
4143186906143186907CCGTGT5GENICheterozygous56961805
4143187744143187745TTAAAAAA2GENIChomozygous56961809
4143188708143188709TA22GENIChomozygous56961813
4143189388143189390GA--19GENICheterozygous56961817
4143190016143190017TC33GENIChomozygous56961821
4143190292143190313CCTAAAAGTAACTTTATCTGG---------------------6GENIChomozygous58082927
4143191441143191442AG20GENIChomozygous56961826
4143191850143191851TA18GENIChomozygous57506945
4143192114143192115GA17GENIChomozygous58082928
4143192203143192204AG10GENIChomozygous56961827
4143192669143192670GA12GENIChomozygous57506947
4143192936143192937GA12GENIChomozygous56961829
4143194567143194568CT15GENIChomozygous57506949
4143195199143195200GT16GENIChomozygous56961831
4143196553143196554AAGT10GENICpossibly homozygous58082929
4143196676143196677TC23GENIChomozygous58082930
4143196922143196923GC38GENIChomozygous56961834
4143199990143199991TG41GENIChomozygous56961838
4143200005143200006GA42GENIChomozygous58082931
4143200339143200340CT39GENIChomozygous58082932
4143201099143201100AC22GENIChomozygous56961840
4143201924143201925TC30GENIChomozygous56961842