chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136130520136130521CT28GENIChomozygous598096578
4136130906136130907TC16GENICpossibly homozygous595626390
4136131674136131675AAG8GENICpossibly homozygous726991082
4136131922136131923GA21GENICpossibly homozygous598096579
4136132029136132030CT9GENIChomozygous595626391
4136132662136132663AT4GENICheterozygous595626392
4136133091136133092GA16GENIChomozygous595626393
4136133344136133345AC7GENIChomozygous595626394
4136133360136133361AG6GENIChomozygous595626395
4136133427136133428TA14GENICheterozygous595626396