chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91554435415544355CT29GENIChomozygous525063067
91554475715544758TC23GENIChomozygous525063068
91554487415544879CCCCC-----12GENICheterozygous692676728
91554487715544879CC--12GENICheterozygous692676729
91554488615544890CCCA----14GENIChomozygous692676730
91554516915545170CCT15GENICpossibly homozygous692676731
91554519415545195CT22GENICheterozygous525063069
91554522415545225GA28GENICpossibly homozygous525063070
91554559415545595GA32GENIChomozygous525063071
91554595115545952CCCA33GENIChomozygous692676732
91554598715545988AG49GENIChomozygous525063072
91554634515546346CG26GENIChomozygous525063073
91554665215546653AG29GENIChomozygous525063074
91554693215546933GA30GENIChomozygous525063075
91554699615546997AC23GENIChomozygous525063076
91554703415547035AG28GENIChomozygous525063077
91554807515548076GGAC9GENICheterozygous692676733
91554812015548121CA19GENIChomozygous525063078
91554831215548313AG25GENIChomozygous525063079
91554853215548533TC35GENIChomozygous525063080