chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71110810411108105CCT2GENICheterozygous53787381
71110882811108829TC18GENIChomozygous53787382
71110895211108954GG--2GENIChomozygous54301541
71110931511109316AG17GENIChomozygous53787383
71110955911109560CA27GENIChomozygous53787384
71110968711109688CA20GENICpossibly homozygous53787385
71111018011110181AG24GENIChomozygous53787386
71111020511110206CT27GENIChomozygous53787387
71111060611110607GA29GENICpossibly homozygous53787388
71111072411110725CG17GENICpossibly homozygous53787389
71111109311111094TC23GENIChomozygous53787391