chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104615459046154591AG44GENIChomozygous51444202
104615490846154909AT42GENIChomozygous51874917
104615553746155538G-28GENIChomozygous52053164
104615577246155773CT19GENIChomozygous52053166
104615588146155882CT29GENIChomozygous52053168
104615694646156947CCTG5GENICheterozygous51444205
104615731346157314TC40GENIChomozygous51874922
104615774246157743TC28GENICpossibly homozygous51874925
104615827546158276GA43GENIChomozygous51444207
104615850246158503TC39GENIChomozygous51444208
104615851146158512TG39GENIChomozygous51444209
104615852746158528AG35GENIChomozygous52053170
104616053446160535CT43GENIChomozygous52053172
104616094246160943GT34GENIChomozygous52053174
104616126446161265AAC13GENIChomozygous51636702
104616211346162114CG36INTERGENIChomozygous52053176
104616303046163031AAG31INTERGENIChomozygous51636706
104616320746163208AG28INTERGENIChomozygous51636707
104616322446163227AAG---18INTERGENIChomozygous51444210
104616449246164493CT40INTERGENIChomozygous51444211
104616452546164527AA--28INTERGENIChomozygous52053178
104616535446165355TTA29INTERGENIChomozygous52053180
104616676746166768TC41INTERGENIChomozygous51444215
104616704846167049AAG26INTERGENIChomozygous51444216
104616720846167209GGGGGA24INTERGENIChomozygous51444217
104616729646167297TC32INTERGENIChomozygous51444218
104616765146167652CT42INTERGENIChomozygous52053182
104616854646168547TC30INTERGENIChomozygous52053184
104616951546169516GA47INTERGENICpossibly homozygous52053186
104617027446170275AC37INTERGENIChomozygous52053188