chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2125764468125764469TG41GENICheterozygous110005964
2125764479125764480TC45GENICheterozygous110005966
2125764491125764492AC63GENICheterozygous110588319
2125764533125764534CT104GENICheterozygous110005967
2125764534125764535CA103GENICheterozygous110005969
2125764537125764538CA103GENICheterozygous110005971
2125764545125764546CA97GENICheterozygous110005973
2125779585125779586TC21GENICpossibly homozygous110006073
2125827602125827603CT25GENICheterozygous110889917
2125860013125860014TC17GENICheterozygous110889918