chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3123614617123614618CG19GENIChomozygous111692542
3123615409123615410AG21GENIChomozygous111692543
3123615566123615567AG17GENIChomozygous111692544
3123615681123615682TC19GENIChomozygous111692545
3123615702123615703TA21GENIChomozygous111692546
3123615971123615972TC26GENIChomozygous111692547
3123616949123616950AC25GENIChomozygous111692549
3123617218123617219TC8GENIChomozygous111692550
3123617227123617228GA8GENIChomozygous111692551
3123617726123617727GA10GENIChomozygous111692552
3123617732123617733GA9GENIChomozygous111692553
3123617938123617939CT20GENIChomozygous111692554
3123618059123618060CT19GENIChomozygous111692555
3123618317123618318GA18GENIChomozygous111692556
3123618322123618323GA16GENIChomozygous111692557
3123618326123618327CT13GENIChomozygous111692558
3123618795123618796AT16GENIChomozygous111692559
3123618889123618890CG11GENIChomozygous111692560
3123618895123618896TC14GENIChomozygous111692561
3123622042123622043TC17GENIChomozygous111692562
3123623946123623947AT19GENIChomozygous111692563
3123624887123624888AG14GENIChomozygous111692564
3123624930123624931AG18GENIChomozygous111692565
3123624935123624936AT18GENIChomozygous111692566
3123626381123626382AG22GENIChomozygous111692567
3123627659123627660TC15GENIChomozygous111692568
3123627973123627974CT15GENIChomozygous111692569
3123629117123629118CT13GENIChomozygous111692570