chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
136856686268566863A10GENICheterozygous141041606
136858712968587130TC30GENIChomozygous142393474
136858726668587267AG45GENIChomozygous142393475
136858763368587635TT39GENIChomozygous142348807
136858766668587666A36GENIChomozygous142348808
136859049668590497TC52GENIChomozygous143591583
136858692468586925AG38GENIChomozygous143591581
136858660668586607CT52GENIChomozygous143591579
136858680868586809AC14GENIChomozygous143591580
136858911268589113CA58GENIChomozygous143591582
136859093868590939AT51GENIChomozygous139335654
136859316568593166TA10GENICheterozygous143591584
136859316768593168TA10GENICheterozygous143591585
136859316968593170TA11GENIChomozygous143591586
136859317168593172TA11GENIChomozygous142393495
136859317368593174TA11GENIChomozygous142393496
136859317568593176TA11GENIChomozygous142393497
136859317768593178TA11GENIChomozygous142393498
136859317968593180TA11GENIChomozygous142393499
136859336768593368AT37GENIChomozygous143591587
136859383368593834CT33GENIChomozygous143591588
136859470368594704AG53GENIChomozygous142393504
136859613568596136GA25GENIChomozygous143591589
136859631468596315CT15GENIChomozygous143591590
136859750668597507CG51GENIChomozygous143591591
136859173168591733GG21GENIChomozygous143552348
136859635568596356A8GENICpossibly homozygous403342608
136859635568596356AC8GENICheterozygous403342609
136859402968594029G50GENIChomozygous143552349