chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143184329143184330GT17GENIChomozygous57506943
4143185628143185629C-21GENIChomozygous58082926
4143186668143186669TC15GENIChomozygous56961804
4143188708143188709TA23GENIChomozygous56961813
4143187744143187745TTAAAAAAA20GENICpossibly homozygous58342733
4143189389143189390AAAG9GENICheterozygous58467518
4143190016143190017TC23GENIChomozygous56961821
4143190292143190313CCTAAAAGTAACTTTATCTGG---------------------20GENIChomozygous58082927
4143191441143191442AG13GENIChomozygous56961826
4143191850143191851TA18GENIChomozygous57506945
4143192114143192115GA15GENIChomozygous58082928
4143192203143192204AG13GENIChomozygous56961827
4143192669143192670GA12GENIChomozygous57506947
4143192936143192937GA14GENIChomozygous56961829
4143194567143194568CT22GENIChomozygous57506949
4143195199143195200GT22GENIChomozygous56961831
4143196553143196554AAGT22GENIChomozygous58082929
4143196676143196677TC14GENIChomozygous58082930
4143196922143196923GC5GENICheterozygous56961834
4143199990143199991TG18GENIChomozygous56961838
4143200005143200006GA18GENIChomozygous58082931
4143200339143200340CT12GENIChomozygous58082932
4143201099143201100AC16GENIChomozygous56961840
4143201924143201925TC8GENIChomozygous56961842