chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5147796638147796639GT46GENIChomozygous114047344
5147796956147796957AG48GENIChomozygous114047350
5147797659147797660GC39GENIChomozygous114047354
5147798437147798438AG11GENICheterozygous114153112
5147798585147798586CT45GENIChomozygous114153113
5147799061147799062GA60GENIChomozygous114047366
5147800993147800994CA64GENIChomozygous114153114
5147801429147801430TC47GENICpossibly homozygous114047372
5147803326147803327GA37GENICpossibly homozygous114047376
5147803443147803444AT41GENIChomozygous114047378