chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124425609944256100CA16GENIChomozygous115336780
124425642044256421CT20GENIChomozygous115336782
124425724044257241CT12GENIChomozygous115390348
124425727344257274GC18GENIChomozygous115336786
124425730544257306TG19GENIChomozygous115336788
124425747844257479GA10GENIChomozygous115336790
124425868644258687TC12GENIChomozygous115336794
124426302344263024GA27GENIChomozygous115390352
124426523344265234AG17GENIChomozygous115390354
124426534544265346CT22GENIChomozygous115336796
124426899844268999GA22GENIChomozygous115390358
124427190544271906CT21GENICheterozygous115390360
124427477744274778GA20GENIChomozygous115430138
124427480944274810GA17GENIChomozygous115390362
124427571144275712CT19GENIChomozygous115390364
124427601344276014CT18GENIChomozygous115336806
124427619344276194TC16GENIChomozygous115390366
124427654244276543GA27GENIChomozygous115336810
124427697844276979GA20GENIChomozygous115336814
124427723444277235AC20GENIChomozygous115336816