chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108917499289174993AG38GENIChomozygous51536718
108917546089175461TC51GENICpossibly homozygous51536719
108917665989176660A-3GENIChomozygous51536722
108917683289176833TTGACA26GENIChomozygous51536723
108917993389179934GC42INTERGENICpossibly homozygous51536727
108917993489179935GT42INTERGENIChomozygous51536728
108917998989179990GC41INTERGENIChomozygous51536729
108918008989180090TTC30INTERGENIChomozygous51536730