chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117512831075128311AG47GENIChomozygous115902182
117513866275138663CT46GENIChomozygous118164403
117514409075144091CT28GENICheterozygous118164404
117514412975144130CT37GENICpossibly homozygous116420999
117514443675144437TC51GENIChomozygous115902184
117514480775144808TC23GENIChomozygous115902186
117514496675144967CT21GENICpossibly homozygous115993187
117514545675145457GA39GENICpossibly homozygous115902188
117514551275145513CT35GENIChomozygous115902190
117514563175145632CT47GENIChomozygous115902192
117514571775145718AG49GENIChomozygous115902194