chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4211128513211128514AAGCAAG8GENIChomozygous57073073
4211128995211128996TC15GENICpossibly homozygous57073074
4211129883211129884CT9GENIChomozygous57073075
4211130216211130217AG21GENIChomozygous57073076
4211132366211132367GA21GENICpossibly homozygous57073077
4211132411211132412GA29GENICpossibly homozygous57073078
4211133185211133186TC20GENICpossibly homozygous57073081
4211133325211133326CT22GENIChomozygous57073082