chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185618066056180661CT14GENIChomozygous110361231
185618127456181275GA34GENICpossibly homozygous110361233
185618249356182494CA21GENIChomozygous110542980
185618270256182703TC34GENIChomozygous110361235
185618373056183731GA72GENICheterozygous119533718
185618383756183838CT34GENICheterozygous119533720
185618391656183917AG35GENICheterozygous119495639
185618402256184023AG31GENICheterozygous119495640
185618530056185301TC43GENIChomozygous110361237