chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155089135550891355A23GENICpossibly homozygous129255357
155089281150892812AG24GENIChomozygous112506013
155089306150893062GA20GENIChomozygous112506015
155089377450893774CT9GENIChomozygous129255358
155089582550895826GA18GENIChomozygous112506017
155089653850896539TA26GENIChomozygous112506019
155089787350897874CT18GENIChomozygous112506021
155089857250898573A24GENIChomozygous129255359
155089890650898907AG27GENIChomozygous112506023
155089930050899301G16GENIChomozygous129255360