chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123987358639873587CT10GENIChomozygous50201963
123987368439873685TC15GENIChomozygous50201965
123987432539874327TC--4GENIChomozygous50201967
123987438939874390AG10GENIChomozygous50201969
123987458839874589CT8GENIChomozygous50201971
123987499239874993GA13GENIChomozygous50201973
123987503739875039GT--2GENIChomozygous50201975
123987539739875398AG6GENICheterozygous50201993
123987551239875514TA--5GENIChomozygous50201997
123987580939875810CT12GENIChomozygous50201999
123987776539877766G-3GENICheterozygous50512107
123987921239879213GA10GENICpossibly homozygous50202021
123987949539879496AG8GENIChomozygous50202023
123988071039880711C-11GENIChomozygous50202027
123988134539881346AG13GENIChomozygous50202028
123988148139881482CG14GENICpossibly homozygous50202030