chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161928985019289851AG55GENIChomozygous111946171
161929026119290262GA56GENIChomozygous112052633
161929172319291724GA65GENIChomozygous111946173
161929196319291964GA59GENIChomozygous111946175
161929263519292636GA59GENIChomozygous111946177
161929329819293299TC60GENIChomozygous111946179
161929393219293933TA50GENIChomozygous111946183
161929475219294753AG55GENIChomozygous111946185
161929571319295714TA48GENIChomozygous111946187
161929733419297335AG61GENIChomozygous111946191
161929809019298091AG59GENIChomozygous111946193
161930021819300219GT56GENIChomozygous111946197
161930037619300377CT30GENIChomozygous111946199
161930257019302571CT56GENIChomozygous111946201
161930282819302829TC53GENIChomozygous111751050
161930304219303043TC54GENIChomozygous111946203
161930323519303236GA63GENICpossibly homozygous111946205
161930328219303283TG64GENIChomozygous111946207
161929793419297934ATGCTCGGCACATGTGCCTGG50GENIChomozygous131173672
161930160919301611TT59GENIChomozygous131173673
161929990019299901CG56GENICpossibly homozygous112129188
161930034919300350GA34GENIChomozygous112129190
161930117519301176CG63GENICpossibly homozygous112129192
161930235619302357CG73GENICpossibly homozygous112129194
161930054019300541AG65GENIChomozygous112203264
161930054119300542TC65GENIChomozygous112203266
161929405319294054GC39GENICheterozygous133305141
161930035319300355AC31GENICheterozygous130703090