chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157052691157052692CG21GENIChomozygous112905310
4157056868157056869AG12GENIChomozygous113062801
4157056870157056871GA12GENIChomozygous113062803
4157059245157059246TC9GENIChomozygous112905322
4157060819157060820CT18GENIChomozygous112905323
4157061171157061172AG11GENIChomozygous112905325
4157062260157062261AT22GENIChomozygous112905327
4157062296157062297AG6GENIChomozygous112905329
4157063379157063380GA23GENIChomozygous112905331
4157064664157064665GA24GENIChomozygous112905332
4157064842157064843AG24GENIChomozygous112905334
4157065016157065017AG18GENIChomozygous112905335
4157065231157065232AG16GENIChomozygous112905337
4157065510157065511AG24GENIChomozygous112905338
4157066129157066130GA23GENIChomozygous112905340
4157066168157066169TC17GENIChomozygous112905342
4157069480157069481TA9GENIChomozygous112905347
4157069897157069898AG20GENIChomozygous112905349
4157070459157070460TG14GENIChomozygous112905351
4157070677157070678TC16GENIChomozygous112905353
4157070792157070793GT13GENICheterozygous112905354
4157070848157070849AG26GENIChomozygous112905356
4157070924157070925TA15GENIChomozygous112905358
4157071047157071048CT21GENIChomozygous112905360
4157071351157071352TC20GENIChomozygous112905362
4157071532157071533GC20GENIChomozygous112905364
4157071613157071614CT21GENIChomozygous112905366
4157071808157071809CT3GENICheterozygous113473828
4157072455157072456GA9GENIChomozygous112905368
4157072963157072964GA10GENIChomozygous112905370
4157073027157073028GT25GENIChomozygous112905372
4157074221157074222CT22GENIChomozygous112905374
4157074875157074876GA14GENIChomozygous112905376
4157075180157075181AG17GENIChomozygous112905378