chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227802623227802624TTA21GENICpossibly homozygous61105912
1227803291227803292T-25GENIChomozygous61105913
1227804290227804292CC--18GENICpossibly homozygous61105914
1227804291227804292C-18GENICheterozygous61105915
1227804718227804719CT22GENIChomozygous61105916
1227807011227807012CCTT14GENIChomozygous61105918
1227807777227807778TC16GENIChomozygous61105919
1227810355227810356A-14GENIChomozygous61105920
1227810782227810783TC14GENIChomozygous61105921
1227813358227813359CT21GENIChomozygous61105922
1227814342227814343AC19GENIChomozygous61105923
1227814653227814654GGA9GENIChomozygous61105924
1227816242227816248CTCTCT------8GENICheterozygous62331390
1227816246227816248CT--8GENICheterozygous62201937
1227817448227817449TC14GENIChomozygous61105925
1227818941227818942GGCTCTTTCGCTCTCTCT3GENIChomozygous62546887
1227819330227819331CG25GENIChomozygous61105927