chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2252307235252307236CT29GENIChomozygous111038423
2252307588252307589AT31GENIChomozygous111038425
2252308075252308076TG40GENIChomozygous111038427
2252308259252308260CT28GENICpossibly homozygous111038429
2252308773252308774TC23GENIChomozygous111038431
2252308785252308786AG28GENIChomozygous111038433
2252308815252308816CG35GENIChomozygous110388698
2252309724252309725AG30GENIChomozygous111038435
2252310028252310029GT28GENIChomozygous111038437
2252310077252310078GA17GENIChomozygous111038439
2252310485252310486CT37GENIChomozygous111038441
2252310617252310618GC25GENIChomozygous111038443
2252310659252310660TG28GENIChomozygous111038445
2252311682252311683GA29GENIChomozygous111038447
2252311727252311728CG35GENIChomozygous111038449
2252312587252312588TC25GENICpossibly homozygous111038452
2252313243252313244GT26GENIChomozygous111038456
2252313658252313659AG17GENIChomozygous110388706
2252314370252314371AT26GENIChomozygous111038458
2252316644252316645TA24GENIChomozygous110854564
2252317225252317226GA19GENIChomozygous110388710
2252318546252318547AG17GENIChomozygous111038460
2252319428252319429CT22GENIChomozygous111038462