chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5124411237124411237A38GENICpossibly homozygous137338692
5124411634124411635CA57GENIChomozygous137610146
5124412414124412415AT59GENIChomozygous137610147
5124413057124413057A65GENIChomozygous137338693
5124413364124413365CT73GENIChomozygous137610148
5124414031124414032AG56GENIChomozygous137610149
5124415798124415799AG79GENIChomozygous137610150