chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1211249164211249165AG14GENIChomozygous875790756
1211250496211250497TC20GENIChomozygous875790757
1211250622211250623CG27GENIChomozygous875790758
1211250971211250972AC18GENIChomozygous875790759
1211251987211251988GA6GENIChomozygous875790760
1211252068211252069CT9GENIChomozygous875790761
1211252076211252077AC7GENIChomozygous875790762
1211252203211252204AG10GENIChomozygous875790763
1211254118211254119AT24GENIChomozygous875790764
1211254143211254144CT13GENIChomozygous875790765
1211254145211254146CT9GENIChomozygous875790766
1211254496211254497CT13GENIChomozygous875790767
1211254854211254855CG27GENIChomozygous875790768
1211255440211255441GT14GENIChomozygous875790769
1211255616211255617AT12GENIChomozygous875790770
1211256722211256723TC22GENIChomozygous875790771
1211257074211257075AG16GENIChomozygous875790772
1211257451211257452CT4GENIChomozygous875790773
1211257827211257828TA5GENIChomozygous875790774
1211258803211258804TC9GENIChomozygous875790775
1211259421211259422AG11GENIChomozygous875790776
1211259737211259738AG17GENIChomozygous875790777
1211260475211260476CG9GENIChomozygous875790778
1211261278211261279AG23GENIChomozygous875790779
1211261430211261431CT12GENIChomozygous875790780
1211262513211262514GA27GENIChomozygous875790781
1211262865211262866AG29GENIChomozygous875790782
1211264098211264099TG10GENIChomozygous875790783