chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51705657217056573AG23GENIChomozygous114473408
51705671217056713AG7GENIChomozygous114473410
51705770617057707TC17GENIChomozygous114473412
51705793517057936TA13GENIChomozygous113675768
51705812817058129GA25GENIChomozygous114473416
51705857017058571TA15GENIChomozygous114473418
51705860117058602CG14GENIChomozygous113675772
51705866817058669GA20GENIChomozygous114473420
51705874017058741GA23GENIChomozygous114473422
51705923117059232CG15GENIChomozygous113675774
51705933517059336TC17GENIChomozygous114473424
51705956017059561AG8GENIChomozygous113675776
51705956517059566AT8GENIChomozygous113675778
51706003217060033CT21GENIChomozygous114473426
51706053717060538TA16GENIChomozygous114473428
51706154617061547GA6GENIChomozygous114473430