chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135989388135989389AT25GENIChomozygous114018769
5135992151135992152CG29GENIChomozygous114018770
5135992632135992633GT27GENIChomozygous114018771
5135993491135993492TC19GENIChomozygous114018772
5135994697135994698AC25GENIChomozygous114018773
5135994803135994804AT26GENICpossibly homozygous114018774
5135993948135993951AAC31GENIChomozygous128242690
5135993077135993077C19GENIChomozygous128242689