chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1156569555156569556CA38GENIChomozygous60907002
1156569600156569601AC40GENIChomozygous60907003
1156569733156569734GT44GENICpossibly homozygous60907004
1156569927156569928CA33GENIChomozygous60907005
1156570299156570300GT15GENIChomozygous60907006
1156570427156570428TC19GENIChomozygous60907007
1156570431156570432TA21GENIChomozygous60907008