chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174180105541801056GA6GENIChomozygous881679013
174180122841801229TC13GENIChomozygous881679014
174180189941801900GA13GENIChomozygous881679015
174180242041802421GA16GENIChomozygous881679016
174180289541802896TC11GENIChomozygous881679017
174180306441803065GA22GENIChomozygous881679018
174180333141803332AG15GENIChomozygous881679019
174180372341803724AG26GENIChomozygous881679020
174180457941804580CA32GENIChomozygous881679021
174180469141804692AT38GENIChomozygous881679022
174180504941805050AG14GENIChomozygous881679023
174180565341805654GA14GENIChomozygous881679024
174180576041805761TC11GENIChomozygous881679025
174180605241806053GT21GENIChomozygous881679026
174180713241807133CT19GENIChomozygous881679027
174180784941807850TC21GENIChomozygous881679028
174180899641808997AG22GENIChomozygous881679029
174180939941809400CG11GENIChomozygous881679030
174180960641809607CT9GENIChomozygous881679031
174180960741809608TA9GENIChomozygous881679032
174181151941811520TG25GENIChomozygous881679033
174181180041811801TC26GENIChomozygous881679034
174181482641814827GA4GENIChomozygous881679035
174181534741815348AC17GENIChomozygous881679036
174181539541815396GA20GENIChomozygous881679037