chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91554435415544355CT31GENIChomozygous520744656
91554475715544758TC33GENICpossibly homozygous520744657
91554487415544879CCCCC-----5GENICheterozygous691011602
91554487715544879CC--5GENICheterozygous691011603
91554488615544890CCCA----8GENIChomozygous691011604
91554516915545170CCT13GENICheterozygous691011605
91554519415545195CT25GENICheterozygous520744658
91554522415545225GA27GENICpossibly homozygous520744659
91554559415545595GA39GENIChomozygous520744660
91554595115545952CCCA31GENIChomozygous691011606
91554598715545988AG34GENIChomozygous520744661
91554634515546346CG35GENIChomozygous520744662
91554665215546653AG45GENIChomozygous520744663
91554693215546933GA36GENIChomozygous520744664
91554699615546997AC55GENICpossibly homozygous520744665
91554703415547035AG51GENIChomozygous520744666
91554807515548076GGAC13GENICheterozygous691011607
91554812015548121CA23GENIChomozygous520744667
91554831215548313AG35GENIChomozygous520744668
91554853215548533TC37GENIChomozygous520744669