chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107353674273536743CT28GENIChomozygous117016523
107357461473574615CA16GENICpossibly homozygous116800108
107362782573627826AG25GENIChomozygous116635347
107363088773630888AG2GENIChomozygous117064129
107363088973630890AG2GENIChomozygous117064131
107363089673630897CG2GENIChomozygous116635351