chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261495862261495863AT14GENIChomozygous125324771
1261498155261498156CT17GENIChomozygous125324772
1261499516261499517GA27GENIChomozygous125324773
1261499838261499839TC4GENICheterozygous125324774
1261500373261500374CT25GENIChomozygous125324775
1261501604261501605AT13GENIChomozygous125324776
1261501900261501901GA25GENIChomozygous125324777
1261502291261502292GA19GENIChomozygous125324778
1261503738261503739GA18GENIChomozygous125324779
1261504399261504400AG23GENIChomozygous125324780
1261504615261504616AG27GENIChomozygous125324781
1261504670261504671CT18GENIChomozygous125324782
1261505054261505055AC20GENIChomozygous125324783
1261506205261506206TC6GENIChomozygous125324784
1261506813261506814TC18GENIChomozygous125324785
1261507253261507254CT21GENIChomozygous125324786
1261507666261507667TA24GENIChomozygous125324787
1261508300261508301CA22GENIChomozygous125324788
1261509652261509653CT17GENIChomozygous125324789
1261510733261510734GA7GENIChomozygous125324790
1261511561261511562CA27GENIChomozygous125324791
1261511784261511785GA6GENIChomozygous125324792
1261511968261511969GA24GENIChomozygous125324793
1261512538261512539CT18GENIChomozygous125324794
1261514005261514006AG11GENIChomozygous125324795