chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7132651895132651896G-12GENIChomozygous54120901
7132651898132651899TG12GENIChomozygous54120902
7132653138132653139CT14GENIChomozygous54120903
7132653290132653291AG22GENICpossibly homozygous54120904
7132653857132653858GA7GENICpossibly homozygous54120905
7132653997132653998TC16GENIChomozygous54120906
7132654262132654263AG17GENIChomozygous54120907
7132655294132655295CT10GENIChomozygous54120908
7132655378132655379GA5GENIChomozygous54120909
7132655774132655775CT19GENICpossibly homozygous54120910
7132656036132656037CT17GENIChomozygous54120911