chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186877412568774126TC32GENIChomozygous46744470
186877543868775439GGGT21GENICpossibly homozygous46667694
186877655368776554GA50GENIChomozygous46744471
186877685268776853A-41GENIChomozygous46506605
186877692368776924TC68GENICpossibly homozygous46744472
186877980968779810AG36GENIChomozygous46744473
186877995068779951T-34GENIChomozygous46744474
186878234868782349TC38GENIChomozygous46744475
186878396168783962TC30GENIChomozygous46744476
186878528268785283CT23GENIChomozygous46744477
186878540668785407GGA37GENIChomozygous46744478
186878585168785852GA40GENIChomozygous46744479
186878625968786260GA29GENIChomozygous46744480
186878634268786343GA35GENIChomozygous46744481
186878668868786689CT52GENIChomozygous46744482
186878697568786976TG35GENIChomozygous46744483
186878858168788582CT38GENIChomozygous46744484
186878965168789652CT46GENIChomozygous46744485
186879248468792485AAG56GENIChomozygous46744486
186879370868793709AG37GENICpossibly homozygous46744487
186879599268795993AC44GENIChomozygous46744488
186879694068796941AC41GENICpossibly homozygous46744489
186879864568798646CT36GENIChomozygous46744490
186879889568798896TC45GENIChomozygous46744491
186879894768798948AG45GENIChomozygous46744492