chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117042314117042315GT21GENIChomozygous115846155
7117043615117043616TC28GENIChomozygous115846157
7117046238117046239TG20GENIChomozygous115846159
7117046634117046635TG16GENIChomozygous115846175
7117046642117046643GC8GENIChomozygous115846177
7117046643117046644TA9GENIChomozygous115846179
7117048001117048002TC16GENIChomozygous115846181
7117049277117049278CT4GENIChomozygous126602098
7117050544117050545AG4GENIChomozygous115846187
7117051084117051085GA7GENIChomozygous115846189
7117052103117052104GA4GENIChomozygous115846195
7117053228117053229GA20GENIChomozygous115846197
7117053322117053323CT17GENIChomozygous115846199
7117054348117054349AG17GENIChomozygous115846201
7117058574117058575GA18GENIChomozygous115846203
7117061618117061619GA12GENIChomozygous115846205
7117054371117054372GT5GENICheterozygous126619970