chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264095442264095443AG26GENIChomozygous957106486
1264095886264095887AG27GENIChomozygous957106487
1264097432264097433TC16GENIChomozygous957106488
1264097682264097683GA28GENIChomozygous957106489
1264099882264099883CT26GENIChomozygous957106490
1264099931264099932CT28GENIChomozygous957106491
1264100059264100060TA28GENIChomozygous957106492
1264100188264100189AG22GENIChomozygous957106493
1264100432264100433GA22GENIChomozygous957106494
1264100637264100638TC23GENIChomozygous957106495
1264100851264100852AG24GENIChomozygous957106496
1264100853264100854AT24GENIChomozygous957106497
1264101725264101726TA26GENIChomozygous957106498
1264101841264101842AG23GENIChomozygous957106499
1264102013264102014GA23GENIChomozygous957106500
1264102022264102023CT18GENIChomozygous957106501
1264102091264102092GA26GENIChomozygous957106502
1264102112264102113TC27GENIChomozygous957106503
1264102373264102374GA19GENIChomozygous957106504
1264102418264102419TC20GENIChomozygous957106505
1264102632264102633CT18GENIChomozygous957106506
1264103285264103286AG6GENIChomozygous957106507
1264103682264103683CT29GENIChomozygous957106508
1264104414264104415GA21GENIChomozygous957106509
1264105443264105444AC17GENIChomozygous957106510