chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2231870071231870072TC23GENIChomozygous110303565
2231870205231870206CA26GENIChomozygous110303573
2231870702231870703GA17GENIChomozygous110303575
2231871874231871875TG23GENIChomozygous110303577
2231873258231873259CA30GENIChomozygous120219243
2231873725231873726TG13GENIChomozygous110303579
2231873739231873740CG14GENIChomozygous110303581
2231874357231874358CT20GENIChomozygous110303583
2231874376231874377AG20GENIChomozygous110303584
2231874715231874716CG30GENIChomozygous110303586
2231874884231874885GA22GENIChomozygous110303588
2231875010231875011AG24GENIChomozygous110303590
2231875119231875120TC32GENIChomozygous110303592
2231875157231875158CG27GENIChomozygous110303594
2231875574231875575TC27GENIChomozygous110303596
2231876583231876584AG27GENIChomozygous110303599
2231876617231876618AC23GENIChomozygous110303601
2231877341231877342GA42GENIChomozygous110303603
2231878076231878077TC11GENIChomozygous110303605
2231878190231878191GC20GENIChomozygous110303607
2231878361231878362AG21GENIChomozygous110303609
2231878722231878723AC27GENIChomozygous110303613
2231878746231878747AT28GENIChomozygous110303615
2231879417231879418CT15GENIChomozygous110303617
2231879474231879475GA22GENIChomozygous110303619
2231879795231879796GA21GENIChomozygous120254674
2231881060231881061TC21GENICpossibly homozygous110303621
2231881080231881081TC20GENICpossibly homozygous110303623
2231881376231881377TG24GENIChomozygous110303625
2231881434231881435CT19GENIChomozygous110303627
2231881496231881497CT24GENIChomozygous110303629