chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124037510840375109AG14GENIChomozygous50203429
124037712440377125CT9GENICpossibly homozygous50203430
124037810140378102TC7GENICheterozygous50203431
124038187440381875TTACAC1GENIChomozygous50203436
124038203840382039T-15GENICpossibly homozygous50203437
124038262240382623CT9GENIChomozygous50203438
124038436640384374GACCACAC--------1GENIChomozygous50203439