chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123987477739874778AG26GENIChomozygous50380989
123987508339875084AATATGTGTGCCTGTC12GENIChomozygous50512103
123987523339875257TGTCTGTGTATGTGTGTGTGTCTG------------------------50GENICheterozygous50571471
123987535039875351GGTC50GENICpossibly homozygous50201989
123987539739875398AG44GENIChomozygous50201993
123987551239875514TA--37GENIChomozygous50201997
123987598939875991AA--21GENICheterozygous50323165
123987599039875991A-21GENICheterozygous50202005
123987643439876435CT23GENIChomozygous50512105
123987679239876800TCATAAAT--------21GENIChomozygous50571473
123987725339877254A-14GENIChomozygous50380996
123987776439877766GG--24GENICheterozygous50571474
123987776539877766G-24GENICpossibly homozygous50512107
123987825339878254CCAAAAAAAAAAAAA4GENIChomozygous50563451
123987825839878259GGA4GENIChomozygous50571476
123987827539878276A-3GENIChomozygous50202013
123987841339878414TTACACACACACAC17GENIChomozygous50571478
123987860439878611AAAAAAA-------14GENICheterozygous50571479
123987860539878611AAAAAA------14GENICheterozygous50571481
123987927139879272TG20GENIChomozygous50380997
123987949539879496AG22GENIChomozygous50202023
123987991339879914TC14GENIChomozygous50380998
123988020939880213ACAC----5GENICheterozygous50571482
123988071039880711C-31GENIChomozygous50202027
123988148139881482CG29GENIChomozygous50202030