chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105553348655533487GT51GENIChomozygous116934827
105553466355534664GA38GENIChomozygous116934829
105553480855534809CT39GENIChomozygous116934831
105553676655536767G19GENIChomozygous131094342
105553686955536871CC25GENIChomozygous131094343
105553768655537687GA40GENIChomozygous116934833
105553778355537784CA28GENICpossibly homozygous116934835
105553795355537954CT39GENIChomozygous116934837
105553677755536777T23GENIChomozygous130681842
105553746955537473AAGA32GENIChomozygous128818953
105553986655539867GA55GENIChomozygous116934839
105554048755540488CT66GENIChomozygous116782610
105554318955543190CT68GENIChomozygous116602555
105554416755544168CT59GENICpossibly homozygous116934841
105554506855545069CG33GENICheterozygous133568363
105554507255545073TG34GENICheterozygous133761628
105554512455545125TC41GENIChomozygous116602557