chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5157821884157821885TC44GENIChomozygous114070486
5157822249157822250TC39GENIChomozygous114070487
5157823493157823494AT40GENICpossibly homozygous114070488
5157824249157824250AT41GENIChomozygous114070489
5157824331157824332GA55GENIChomozygous114070490
5157826521157826522AG35GENIChomozygous114070491
5157826918157826919AC42GENIChomozygous114070492
5157828070157828071GA46GENIChomozygous114070493
5157828072157828073CA46GENIChomozygous114070494
5157828794157828795AG46GENIChomozygous114070495
5157828896157828897TG50GENIChomozygous114070496
5157829333157829334TC35GENIChomozygous114070497
5157829684157829685GA44GENICpossibly homozygous114070498
5157829846157829847GA55GENIChomozygous114070499
5157830714157830715GA66GENIChomozygous114070500
5157831975157831976CT52GENIChomozygous114070501
5157837398157837399CT31GENIChomozygous114070502
5157837449157837450GT34GENIChomozygous114070503
5157837604157837605GA50GENIChomozygous114070504
5157837744157837745GA18GENIChomozygous114070505
5157838325157838326GA42GENIChomozygous114070506
5157839657157839658TC76GENIChomozygous114070507
5157841222157841223CA39GENIChomozygous114070508
5157842985157842986AG48GENIChomozygous114070509
5157846079157846080TC28GENICheterozygous114070510