chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157049467157049468TC5GENIChomozygous112905304
4157049520157049521AG10GENIChomozygous112905308
4157052691157052692CG28GENIChomozygous112905310
4157058363157058364AG9GENIChomozygous112905312
4157058554157058555CA19GENICheterozygous112905314
4157058980157058981AC38GENICheterozygous112905316
4157059245157059246TC17GENIChomozygous112905322
4157061171157061172AG13GENIChomozygous112905325
4157062260157062261AT27GENIChomozygous112905327
4157062296157062297AG18GENIChomozygous112905329
4157063379157063380GA26GENIChomozygous112905331
4157064316157064317CA26GENIChomozygous113184380
4157064664157064665GA16GENIChomozygous112905332
4157064842157064843AG15GENIChomozygous112905334
4157065016157065017AG20GENIChomozygous112905335
4157065231157065232AG27GENIChomozygous112905337
4157065510157065511AG27GENIChomozygous112905338
4157065878157065879GA11GENIChomozygous113184381
4157066168157066169TC26GENIChomozygous112905342
4157066932157066933GA15GENIChomozygous112905344
4157068267157068268TC21GENIChomozygous113184382
4157069122157069123CT13GENIChomozygous112905345
4157069480157069481TA22GENIChomozygous112905347
4157069897157069898AG20GENIChomozygous112905349
4157070459157070460TG24GENIChomozygous112905351
4157070677157070678TC24GENIChomozygous112905353
4157070776157070777TA22GENIChomozygous113184383
4157070792157070793GT18GENIChomozygous112905354
4157070848157070849AG19GENIChomozygous112905356
4157070924157070925TA23GENIChomozygous112905358
4157071047157071048CT30GENIChomozygous112905360
4157071351157071352TC18GENIChomozygous112905362
4157071532157071533GC19GENIChomozygous112905364
4157071613157071614CT23GENIChomozygous112905366
4157072455157072456GA22GENIChomozygous112905368
4157072963157072964GA12GENIChomozygous112905370
4157073027157073028GT25GENIChomozygous112905372
4157073400157073401CT17GENIChomozygous113184384
4157073862157073863AG30GENIChomozygous113184385
4157074875157074876GA24GENIChomozygous112905376
4157075180157075181AG28GENIChomozygous112905378