chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105395979253959793TC21GENIChomozygous142247790
105396136353961364GT22GENIChomozygous145741088
105396157253961573GA13GENIChomozygous145741089
105396638153966382A24GENICpossibly homozygous140902939
105396660653966607GA23GENIChomozygous145741090
105396919553969197CT19GENICpossibly homozygous142203359
105397057253970573CG16GENICpossibly homozygous146958934
105397057253970573C16GENICheterozygous404015000
105397057453970575CG19GENICheterozygous146958935
105397060553970606A11GENICheterozygous403286911
105397060553970606AT11GENICheterozygous403286912
105397216853972169GA28GENIChomozygous145741091
105397461653974616A27GENIChomozygous145729574