chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5157821705157821705G37GENIChomozygous128263037
5157821884157821885TC39GENIChomozygous114070486
5157821899157821903AAAC39GENIChomozygous128263038
5157822249157822250TC55GENIChomozygous114070487
5157822255157822256G57GENIChomozygous128263039
5157823493157823494AT66GENIChomozygous114070488
5157824249157824250AT53GENIChomozygous114070489
5157824331157824332GA61GENIChomozygous114070490
5157825535157825538TTT45GENIChomozygous128263040
5157826521157826522AG61GENIChomozygous114070491
5157826918157826919AC44GENIChomozygous114070492
5157828070157828071GA49GENIChomozygous114070493
5157828072157828073CA49GENIChomozygous114070494
5157828676157828677T37GENIChomozygous128263041
5157828794157828795AG46GENIChomozygous114070495
5157828896157828897TG42GENICpossibly homozygous114070496
5157829333157829334TC41GENIChomozygous114070497
5157829684157829685GA41GENIChomozygous114070498
5157829846157829847GA52GENIChomozygous114070499
5157830058157830058T50GENIChomozygous128263042
5157830714157830715GA53GENIChomozygous114070500
5157831975157831976CT62GENIChomozygous114070501
5157837398157837399CT34GENIChomozygous114070502
5157837449157837450GT36GENIChomozygous114070503
5157837604157837605GA56GENIChomozygous114070504
5157837744157837745GA30GENIChomozygous114070505
5157838325157838326GA49GENIChomozygous114070506
5157839657157839658TC45GENIChomozygous114070507
5157841222157841223CA52GENIChomozygous114070508
5157842985157842986AG54GENIChomozygous114070509
5157846079157846079C36GENICpossibly homozygous128263044