chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
52443431324434314GC23GENIChomozygous119008862
52443441624434417CT35GENIChomozygous118970463
52443445824434459CG41GENIChomozygous119008863
52443475624434757CT32GENIChomozygous119201039
52443495924434960AG33GENIChomozygous118970465
52443752324437524TC50GENIChomozygous118970467
52443759324437594TC48GENIChomozygous118970469
52443814124438142TC53GENICpossibly homozygous118970471
52443820424438205GA57GENICpossibly homozygous118970473
52443850424438505TG47GENICpossibly homozygous118970475
52443876024438761TA49GENIChomozygous118970477
52443984524439846TC62GENIChomozygous118970479
52444022024440221TC56GENIChomozygous118970481
52444060524440606TG50GENIChomozygous118970483
52444130224441303TC40GENIChomozygous119008864
52444156224441563CG54GENIChomozygous118970485
52444336024443361GA44GENIChomozygous118970487
52444631024446311GA51GENIChomozygous118970489
52444635024446350AC54GENIChomozygous130951413
52443713024437134CTTA55GENIChomozygous130951408
52443919624439196C54GENICpossibly homozygous130951409
52444347924443479A40GENIChomozygous130951410
52444545924445459GG36GENIChomozygous130951411
52444630224446302A49GENIChomozygous130951412
52443836624438367CT50GENIChomozygous119143877
52444130024441301TC32GENICpossibly homozygous119143879