chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2231870205231870206CA28GENIChomozygous110303573
2231870702231870703GA32GENIChomozygous110303575
2231871874231871875TG26GENIChomozygous110303577
2231873725231873726TG18GENIChomozygous110303579
2231873739231873740CG16GENIChomozygous110303581
2231874357231874358CT24GENIChomozygous110303583
2231874376231874377AG25GENIChomozygous110303584
2231874715231874716CG25GENIChomozygous110303586
2231874884231874885GA16GENIChomozygous110303588
2231875010231875011AG19GENIChomozygous110303590
2231875119231875120TC22GENIChomozygous110303592
2231875157231875158CG28GENIChomozygous110303594
2231875574231875575TC26GENIChomozygous110303596
2231876583231876584AG25GENIChomozygous110303599
2231876617231876618AC23GENIChomozygous110303601
2231877341231877342GA30GENIChomozygous110303603
2231878076231878077TC33GENIChomozygous110303605
2231878190231878191GC39GENIChomozygous110303607
2231878361231878362AG27GENIChomozygous110303609
2231878490231878491CT26GENIChomozygous110303611
2231878722231878723AC35GENIChomozygous110303613
2231878746231878747AT35GENIChomozygous110303615
2231879417231879418CT24GENIChomozygous110303617
2231879474231879475GA19GENIChomozygous110303619
2231881060231881061TC27GENIChomozygous110303621
2231881080231881081TC27GENIChomozygous110303623
2231881376231881377TG19GENIChomozygous110303625
2231881434231881435CT17GENIChomozygous110303627
2231881496231881497CT14GENIChomozygous110303629