chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123987385039873851TC17GENIChomozygous50380988
123987432539874327TC--10GENICpossibly homozygous50201967
123987438939874390AG26GENICpossibly homozygous50201969
123987458839874589CT21GENIChomozygous50201971
123987499239874993GA25GENICheterozygous50201973
123987503739875039GT--1GENIChomozygous50201975
123987539739875398AG11GENICheterozygous50201993
123987551239875514TA--8GENIChomozygous50201997
123987580939875810CT23GENICpossibly homozygous50201999
123987776539877766G-4GENIChomozygous50512107
123987921239879213GA16GENICpossibly homozygous50202021
123987949539879496AG9GENIChomozygous50202023
123988071039880711C-12GENIChomozygous50202027
123988148139881482CG15GENIChomozygous50202030
123987641439876415GA11GENIChomozygous50421941