chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123987477739874778AG6GENIChomozygous50380989
123987503739875039GT--1GENIChomozygous50201975
123987507239875073TTGC1GENIChomozygous50380990
123987508339875084AATATGTGTGCCTGTC7GENIChomozygous50512103
123987523339875257TGTCTGTGTATGTGTGTGTGTCTG------------------------59GENICheterozygous50571471
123987535039875351GGTC43GENICpossibly homozygous50201989
123987539739875398AG34GENIChomozygous50201993
123987551239875514TA--44GENIChomozygous50201997
123987598939875991AA--20GENICheterozygous50323165
123987599039875991A-20GENICheterozygous50202005
123987643439876435CT19GENICpossibly homozygous50512105
123987679239876800TCATAAAT--------24GENIChomozygous50571473
123987725339877254A-17GENICpossibly homozygous50380996
123987776439877766GG--16GENICheterozygous50571474
123987776539877766G-16GENICpossibly homozygous50512107
123987825839878259GGA1GENIChomozygous50571476
123987841339878414TTACACACACACAC17GENIChomozygous50571478
123987860439878611AAAAAAA-------11GENICheterozygous50571479
123987860539878611AAAAAA------11GENICheterozygous50571481
123987927139879272TG16GENIChomozygous50380997
123987949539879496AG30GENIChomozygous50202023
123987991339879914TC16GENIChomozygous50380998
123988071039880711C-18GENIChomozygous50202027
123988148139881482CG25GENIChomozygous50202030