chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261495333261495334AG15GENIChomozygous125383025
1261495449261495450AC11GENIChomozygous125383026
1261496445261496446GA13GENIChomozygous125383027
1261496570261496571AT4GENIChomozygous125383028
1261496574261496575TA5GENIChomozygous125383029
1261496619261496620GA17GENIChomozygous125383030
1261496841261496842GA17GENIChomozygous125383031
1261499416261499417GT28GENIChomozygous125383032
1261499452261499453AG21GENIChomozygous125383033
1261499516261499517GA28GENIChomozygous125324773
1261499838261499839TC4GENICheterozygous125324774
1261500092261500093AG17GENIChomozygous125383034
1261500175261500176CT23GENIChomozygous125383035
1261500373261500374CT18GENIChomozygous125324775
1261500676261500677AC26GENIChomozygous125383036
1261501604261501605AT16GENIChomozygous125324776
1261501914261501915TA12GENIChomozygous125383037
1261503772261503773CT14GENIChomozygous125383038
1261504143261504144GA4GENIChomozygous125383039
1261504399261504400AG19GENIChomozygous125324780
1261504615261504616AG15GENIChomozygous125324781
1261504670261504671CT11GENIChomozygous125324782
1261506205261506206TC6GENIChomozygous125324784
1261506813261506814TC15GENIChomozygous125324785
1261508031261508032AG5GENIChomozygous125383040
1261508385261508386GA15GENIChomozygous125383041
1261508414261508415GA22GENIChomozygous125383042
1261508968261508969GA7GENIChomozygous125383043
1261509652261509653CT8GENIChomozygous125324789
1261509732261509733AG5GENIChomozygous125383044
1261509971261509972GA9GENIChomozygous125383045
1261510029261510030TG6GENICheterozygous125383046
1261511561261511562CA23GENIChomozygous125324791