chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174180105541801056GA6GENIChomozygous111048972
174180122841801229TC13GENIChomozygous111048974
174180189941801900GA13GENIChomozygous111048976
174180242041802421GA16GENIChomozygous111048978
174180289541802896TC11GENIChomozygous111048980
174180306441803065GA22GENIChomozygous111048982
174180333141803332AG15GENIChomozygous111048984
174180372341803724AG26GENIChomozygous111048986
174180457941804580CA32GENIChomozygous111048988
174180469141804692AT38GENIChomozygous111048990
174180504941805050AG14GENIChomozygous111048992
174180565341805654GA14GENIChomozygous111048994
174180576041805761TC11GENIChomozygous111048996
174180605241806053GT21GENIChomozygous111048998
174180713241807133CT19GENIChomozygous111049000
174180784941807850TC21GENIChomozygous111049002
174180899641808997AG22GENIChomozygous111049004
174180939941809400CG11GENIChomozygous111049006
174180960641809607CT9GENIChomozygous111049008
174180960741809608TA9GENIChomozygous111049010
174181151941811520TG25GENIChomozygous111049016
174181180041811801TC26GENIChomozygous111049018
174181482641814827GA4GENIChomozygous111049020
174181534741815348AC17GENIChomozygous111049022
174181539541815396GA20GENIChomozygous111049024