chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103929802739298028CA26GENIChomozygous893741170
103930015839300159TC4GENIChomozygous893741171
103930322039303221GT24GENIChomozygous893741172
103930533339305334AG6GENIChomozygous893741173
103930810739308108AG17GENIChomozygous893741174
103930858339308584AC28GENIChomozygous893741175
103931018539310186CT4GENIChomozygous893741176
103931030739310308CT12GENIChomozygous893741177
103931064539310646CT11GENIChomozygous893741178
103931405139314052TC4GENIChomozygous893741179
103931430539314306CA14GENIChomozygous893741180
103931528839315289AG20GENIChomozygous893741181
103931578939315790CT25GENIChomozygous893741182
103931628839316289TC20GENIChomozygous893741183
103931691439316915CT14GENIChomozygous893741184
103931697239316973TG7GENIChomozygous893741185
103931697739316978CT9GENIChomozygous893741186
103931718139317182AC17GENICheterozygous893741187
103931744539317446GC13GENIChomozygous893741188
103931745639317457GA18GENIChomozygous893741189
103931766839317669AC5GENIChomozygous893741190
103931782539317826AT29GENIChomozygous893741191
103931803639318037CT21GENIChomozygous893741192