chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135209311752093118TG69GENIChomozygous980166155
135209358352093584GA42GENIChomozygous980166156
135209401952094020CT61GENIChomozygous980166157
135209457352094574CT31GENIChomozygous980166158
135209478952094790TC45GENIChomozygous980166159
135209546852095469CT43GENICpossibly homozygous980166160
135209575552095756CT50GENIChomozygous980166161
135209591152095912AC55GENIChomozygous980166162
135209591252095913GA55GENIChomozygous980166163
135209750152097502CT47GENIChomozygous980166164
135209885352098854TC28GENIChomozygous980166165
135209892652098927TG33GENIChomozygous980166166
135210154452101545GT83GENIChomozygous980166167
135210237252102373AT41GENIChomozygous980166168
135210270752102708TC65GENIChomozygous980166169
135210476652104767GA35GENIChomozygous980166170
135210583452105835TC39GENIChomozygous980166171
135210597752105978TC35GENIChomozygous980166172
135210604052106041TC45GENIChomozygous980166173
135210716152107162AT55GENIChomozygous980166174
135210756652107567GA46GENIChomozygous980166175
135210780152107802TG38GENIChomozygous980166176
135210825352108254AC33GENIChomozygous980166177
135210861652108617TC67GENIChomozygous980166178
135210910752109108AT34GENIChomozygous980166179
135210912952109130TA32GENIChomozygous980166180
135210918252109183CT34GENIChomozygous980166181
135210927752109278AG28GENIChomozygous980166182
135210985352109854TC34GENIChomozygous980166183
135211076752110768GA64GENIChomozygous980166184
135211139952111400AC63GENIChomozygous980166185
135211150052111501GA21GENIChomozygous980166186