chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123987477739874778AG19GENIChomozygous50380989
123987508339875084AATATGTGTGCCTGTC12GENIChomozygous50512103
123987523339875257TGTCTGTGTATGTGTGTGTGTCTG------------------------40GENICheterozygous50571471
123987535039875351GGTC43GENICpossibly homozygous50201989
123987539739875398AG34GENIChomozygous50201993
123987551239875514TA--36GENIChomozygous50201997
123987598939875991AA--11GENICheterozygous50323165
123987643439876435CT17GENICpossibly homozygous50512105
123987679239876800TCATAAAT--------21GENIChomozygous50571473
123987725339877254A-15GENIChomozygous50380996
123987776539877766G-18GENIChomozygous50512107
123987825339878254CCAAAAAAAAAAAAA4GENIChomozygous50563451
123987825839878259GGA4GENIChomozygous50571476
123987827539878276A-4GENIChomozygous50202013
123987841339878414TTACACAC13GENICheterozygous50604468
123987841339878414TTACACACACACAC13GENICpossibly homozygous50571478
123987860439878611AAAAAAA-------12GENICheterozygous50571479
123987860539878611AAAAAA------12GENICpossibly homozygous50571481
123987927139879272TG23GENIChomozygous50380997
123987949539879496AG14GENIChomozygous50202023
123987991339879914TC13GENIChomozygous50380998
123988020739880213ACACAC------9GENICheterozygous50655138
123988020939880213ACAC----9GENICheterozygous50571482
123988071039880711C-38GENIChomozygous50202027
123988148139881482CG29GENIChomozygous50202030