chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51705657217056573AG36GENIChomozygous114473408
51705671217056713AG37GENIChomozygous114473410
51705770617057707TC13GENIChomozygous114473412
51705775717057758GT13GENIChomozygous114473414
51705793517057936TA10GENIChomozygous113675768
51705812817058129GA15GENIChomozygous114473416
51705857017058571TA9GENIChomozygous114473418
51705860117058602CG13GENIChomozygous113675772
51705874017058741GA13GENIChomozygous114473422
51705923117059232CG39GENIChomozygous113675774
51705933517059336TC31GENIChomozygous114473424
51705956017059561AG29GENIChomozygous113675776
51705956517059566AT30GENIChomozygous113675778
51706003217060033CT25GENIChomozygous114473426
51706053717060538TA39GENIChomozygous114473428
51706154617061547GA35GENIChomozygous114473430