chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1768857546885755AT35GENICpossibly homozygous110941980
1768861036886104TC41GENIChomozygous110941982
1768891766889177AG49GENIChomozygous110941984
1768905256890526TC28GENIChomozygous110941986
1768911226891123CT52GENIChomozygous110941990
1768912716891272TC41GENIChomozygous110941992