chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135988790135988791TG46GENIChomozygous114442854
5135989388135989389AT49GENIChomozygous114018769
5135989522135989523AT53GENIChomozygous114442856
5135990000135990001AC87GENIChomozygous114442858
5135990642135990643CA28GENIChomozygous114442860
5135992632135992633GT35GENIChomozygous114018771
5135994697135994698AC69GENICpossibly homozygous114018773
5135994803135994804AT34GENIChomozygous114018774