chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
78160735781607358TC30GENIChomozygous967131168
78160740681607407TC24GENIChomozygous967131169
78160741481607415TC22GENICpossibly homozygous967131170
78160754081607541AG32GENICpossibly homozygous967131171
78160779481607795TG32GENIChomozygous967131172
78160803481608035TA8GENIChomozygous967131173
78160871681608717CG38GENICpossibly homozygous967131174
78160879281608793TC29GENIChomozygous967131175
78160917081609171TC21GENIChomozygous967131176
78160926581609266CT36GENICpossibly homozygous967131177
78160990781609908TG31GENIChomozygous967131178
78161014981610150TC22GENIChomozygous967131179
78161021481610215GA25GENIChomozygous967131180
78161033681610337GA25GENIChomozygous967131181
78161040981610410TA20GENIChomozygous967131182
78161077981610780AG37GENIChomozygous967131183
78161216681612167AG26GENICpossibly homozygous967131184
78161254881612549AG33GENIChomozygous967131185
78161269081612691AG33GENICpossibly homozygous967131186