chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108917499289174993AG25GENIChomozygous51536718
108917546089175461TC13GENICpossibly homozygous51536719
108917632889176329CT13GENICheterozygous52165369
108917658089176581CCG4GENIChomozygous52574197
108917668989176690G-5GENICheterozygous52445299
108917683289176833TTGACA3GENIChomozygous51536723
108917687189176872GA13GENICheterozygous52574199
108917729689177297CT22GENICpossibly homozygous52574202
108917858189178583AG--4INTERGENIChomozygous51536726
108917993389179934GC1INTERGENIChomozygous51536727
108917993489179935GT1INTERGENIChomozygous51536728