chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106157176061571761TA45GENICpossibly homozygous138802370
106157498861574989CT30GENIChomozygous144867342
106157505961575060AG9GENIChomozygous145149046
106157506161575062AG9GENIChomozygous145149047
106157507561575076GA9GENIChomozygous145149048
106157529761575298TC24GENIChomozygous138802372
106157614461576145TC63GENICpossibly homozygous138802373
106157899661578997AT48GENIChomozygous144867343
106157925661579257AG64GENIChomozygous138802376
106158011261580122AGAGACTCTA48GENIChomozygous144855959
106157511261575120CACACACG5GENIChomozygous145148371
106157519861575200CA8GENIChomozygous144855958
106157643361576434A47GENICpossibly homozygous138686682
106157887561578876A41GENICpossibly homozygous138686683
106158172461581725GA50GENIChomozygous138802382
106158190561581905A57GENIChomozygous144855960
106158328461583285GA34GENIChomozygous144867344
106158492561584926GT65GENICpossibly homozygous144867345
106158888061588881AG44GENIChomozygous138802385
106158899861588999GA40GENIChomozygous144867346
106159323261593233CT44GENIChomozygous144867347
106159328061593281TC41GENIChomozygous138802389
106159623161596232GA4GENIChomozygous138802390
106159623661596237AG7GENICheterozygous144867348
106159624061596241AG6GENICheterozygous144867349
106160226161602262CT51GENIChomozygous144867350
106160403861604039TA42GENICpossibly homozygous138802394
106160559561605596AT33GENIChomozygous138802396
106160715261607153CT44GENIChomozygous144867351