chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135128102251281023CT20GENICpossibly homozygous809057131
135128164151281642CT48GENIChomozygous809057132
135128454951284550AG56GENIChomozygous809057133
135128462651284627AG50GENIChomozygous809057134
135128502551285026GA60GENIChomozygous809057135
135128665151286652CT45GENIChomozygous809057136
135128968151289682TC35GENIChomozygous809057137
135128968251289683TC35GENIChomozygous809057138
135128981451289815GA46GENIChomozygous809057139
135128989251289893TG57GENIChomozygous809057140
135129055851290559TC56GENIChomozygous809057141
135129418651294187CT36GENIChomozygous809057142
135129593851295939GA38GENIChomozygous809057143
135129869351298694GC55GENIChomozygous809057144
135129869451298695GA56GENICpossibly homozygous809057145
135130005751300058CT49GENIChomozygous809057146
135130059651300597GA54GENIChomozygous809057147
135130096351300964AT8GENIChomozygous809057148
135130369251303693TC38GENIChomozygous809057149
135130411551304116GA45GENIChomozygous809057150