chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174180105541801056GA16GENIChomozygous989441017
174180122841801229TC10GENIChomozygous989441018
174180189941801900GA25GENIChomozygous989441019
174180242041802421GA14GENIChomozygous989441020
174180289541802896TC30GENIChomozygous989441021
174180306441803065GA31GENIChomozygous989441022
174180333141803332AG27GENIChomozygous989441023
174180372341803724AG18GENIChomozygous989441024
174180457941804580CA28GENIChomozygous989441025
174180469141804692AT37GENIChomozygous989441026
174180504941805050AG17GENIChomozygous989441027
174180565341805654GA23GENIChomozygous989441028
174180576041805761TC26GENIChomozygous989441029
174180605241806053GT13GENIChomozygous989441030
174180713241807133CT24GENIChomozygous989441031
174180784941807850TC27GENIChomozygous989441032
174180899641808997AG21GENIChomozygous989441033
174180939941809400CG8GENIChomozygous989441034
174180960641809607CT23GENIChomozygous989441035
174180960741809608TA23GENIChomozygous989441036
174181127341811274TC49GENIChomozygous989441037
174181148041811481GA23GENIChomozygous989441038
174181151941811520TG35GENIChomozygous989441039
174181180041811801TC32GENIChomozygous989441040
174181482641814827GA11GENIChomozygous989441041
174181534741815348AC29GENIChomozygous989441042
174181539541815396GA33GENIChomozygous989441043