chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116732257116732258AG19GENIChomozygous116669999
8116734212116734213AG27GENIChomozygous116670003
8116736861116736862AG25GENIChomozygous116670013
8116737839116737840CT19GENIChomozygous117149209
8116740312116740313AG28GENIChomozygous116670025
8116746767116746768CT35GENIChomozygous116670059
8116747054116747055CT35GENICpossibly homozygous117149211
8116747711116747712CG17GENIChomozygous117149212
8116748143116748144CG36GENIChomozygous117149213
8116748664116748665GC26GENIChomozygous117149214
8116749214116749215AG15GENICpossibly homozygous117149215
8116749414116749415CT26GENIChomozygous117149217
8116750338116750339AT27GENIChomozygous116670073