chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264095442264095443AG35GENIChomozygous951543445
1264095886264095887AG19GENIChomozygous951543446
1264097432264097433TC17GENIChomozygous951543447
1264097633264097634AC34GENIChomozygous951543448
1264097682264097683GA25GENIChomozygous951543449
1264099882264099883CT24GENIChomozygous951543450
1264099931264099932CT23GENIChomozygous951543451
1264100059264100060TA26GENIChomozygous951543452
1264100188264100189AG20GENIChomozygous951543453
1264100432264100433GA31GENIChomozygous951543454
1264100637264100638TC38GENIChomozygous951543455
1264100851264100852AG39GENIChomozygous951543456
1264100853264100854AT40GENIChomozygous951543457
1264101191264101192TC22GENIChomozygous951543458
1264101725264101726TA29GENIChomozygous951543459
1264101841264101842AG26GENIChomozygous951543460
1264102013264102014GA26GENIChomozygous951543461
1264102022264102023CT26GENIChomozygous951543462
1264102091264102092GA29GENIChomozygous951543463
1264102112264102113TC31GENIChomozygous951543464
1264102373264102374GA33GENIChomozygous951543465
1264102418264102419TC26GENIChomozygous951543466
1264102632264102633CT33GENIChomozygous951543467
1264103104264103105GA20GENIChomozygous951543468
1264103285264103286AG17GENIChomozygous951543469
1264103682264103683CT26GENIChomozygous951543470
1264104414264104415GA28GENIChomozygous951543471
1264105443264105444AC23GENIChomozygous951543472