chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1211249164211249165AG39GENIChomozygous928147646
1211250496211250497TC50GENIChomozygous928147647
1211250622211250623CG44GENIChomozygous928147648
1211250971211250972AC39GENIChomozygous928147649
1211251987211251988GA36GENIChomozygous928147650
1211252068211252069CT55GENIChomozygous928147651
1211252076211252077AC52GENIChomozygous928147652
1211252203211252204AG31GENIChomozygous928147653
1211254118211254119AT37GENIChomozygous928147654
1211254143211254144CT32GENIChomozygous928147655
1211254145211254146CT30GENIChomozygous928147656
1211254496211254497CT42GENIChomozygous928147657
1211254854211254855CG55GENIChomozygous928147658
1211255440211255441GT32GENIChomozygous928147659
1211255616211255617AT33GENIChomozygous928147660
1211256722211256723TC39GENIChomozygous928147661
1211257074211257075AG22GENIChomozygous928147662
1211258803211258804TC28GENIChomozygous928147663
1211259421211259422AG25GENIChomozygous928147664
1211259737211259738AG58GENIChomozygous928147665
1211260475211260476CG30GENIChomozygous928147666
1211261278211261279AG34GENIChomozygous928147667
1211261430211261431CT39GENIChomozygous928147668
1211262513211262514GA44GENICpossibly homozygous928147669
1211262865211262866AG46GENIChomozygous928147670
1211264098211264099TG33GENIChomozygous928147671