chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
39047485790474858C18GENICpossibly homozygous403071182
39047485790474858CT18GENICheterozygous403071183
39047485990474860CT18GENICheterozygous403071184
39047485990474860C18GENICpossibly homozygous403071185
39047486390474864CT18GENICpossibly homozygous140993880