chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1140756299140756300CA17GENIChomozygous565072159
1140756458140756459AT26GENICpossibly homozygous565072160
1140756502140756503GA22GENIChomozygous565072161
1140756738140756739CG13GENIChomozygous565072162
1140756742140756743TC16GENIChomozygous565072163
1140757180140757181A-4GENIChomozygous707648150
1140757351140757352GA10GENIChomozygous565072164
1140757409140757410GA6GENICheterozygous565072165
1140757487140757488TG18GENIChomozygous565072166
1140757549140757550AT21GENIChomozygous565072167
1140757615140757616TC17GENIChomozygous565072168
1140757729140757730CT8GENIChomozygous565072169
1140757735140757736CT4GENIChomozygous565072170
1140758451140758452TA3GENIChomozygous565072171
1140758794140758795TC6GENIChomozygous565072172
1140758860140758861CCA10GENICpossibly homozygous707648151
1140759215140759216TC6GENICheterozygous565072173
1140759424140759435AGCTTCTGGAG-----------2GENIChomozygous707648152
1140759762140759763CT23GENICpossibly homozygous565072174
1140759973140759974TC3GENIChomozygous565072175
1140759993140759994GT10GENIChomozygous565072176
1140760129140760130AG20GENIChomozygous565072177
1140760294140760295AG16GENIChomozygous565072178
1140760428140760429GA9GENIChomozygous565072179
1140760430140760431AG8GENIChomozygous565072180
1140760698140760699CT19GENIChomozygous565072181
1140760828140760829GA21GENIChomozygous565072182
1140760919140760920CA10GENIChomozygous565072183
1140760987140760988GC21GENIChomozygous565072184
1140761272140761273TTA8GENIChomozygous707648153
1140761329140761330TC17GENIChomozygous565072185
1140761449140761450GA20GENIChomozygous565072186
1140761482140761483GA25GENIChomozygous565072187
1140761833140761834CA18GENIChomozygous565072188