chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71110882811108829TC13GENIChomozygous53787382
71110895211108954GG--6GENICheterozygous54301541
71110931511109316AG10GENICpossibly homozygous53787383
71110955911109560CA17GENICpossibly homozygous53787384
71110968711109688CA17GENICpossibly homozygous53787385
71111018011110181AG20GENIChomozygous53787386
71111020511110206CT11GENIChomozygous53787387
71111060611110607GA20GENICpossibly homozygous53787388
71111072411110725CG6GENICheterozygous53787389
71111109311111094TC9GENIChomozygous53787391