chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2242797892242797893AG19GENIChomozygous110344475
2242798586242798587CA23GENIChomozygous110344486
2242798764242798765GT26GENIChomozygous110344488
2242798986242798987GA28GENIChomozygous110344490
2242800384242800385CG25GENIChomozygous110344492
2242800637242800638AG20GENIChomozygous110344494
2242801415242801416CT18GENIChomozygous110344496
2242801697242801698GA33GENIChomozygous110344498
2242802666242802667TG18GENIChomozygous110344500
2242805576242805577AG33GENICpossibly homozygous110344504
2242806618242806619CT16GENIChomozygous110344506
2242821190242821191GA10GENIChomozygous110344508
2242822644242822645AG24GENIChomozygous110344510
2242824417242824418CA21GENIChomozygous110344512
2242824685242824686GT21GENIChomozygous110344514
2242825068242825069TG13GENIChomozygous110344516
2242825259242825260CT25GENIChomozygous110344518
2242826620242826621AG19GENIChomozygous110344520
2242827816242827817GT9GENICheterozygous111423890
2242828316242828317CG4GENIChomozygous110344524
2242828385242828386GT6GENIChomozygous110344526
2242827231242827232AG8GENICheterozygous125609822