chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3165905776165905777CA1INTERGENIChomozygous79705903
3165921806165921807CT10INTERGENICheterozygous72555570
3165909771165909772GA14INTERGENIChomozygous72555549
3165914850165914851CT12INTERGENIChomozygous72555552
3165921073165921074GA8INTERGENICheterozygous72555555
3165921077165921078TG6INTERGENICheterozygous72555558
3165921079165921080CA5INTERGENIChomozygous72555561
3165921081165921082TA5INTERGENIChomozygous72555564
3165921084165921085CA5INTERGENIChomozygous72555567
3165921810165921811CG10INTERGENICheterozygous72555573
3165921811165921812AG10INTERGENICheterozygous72555576
3165921834165921835CA7INTERGENICpossibly homozygous72555579
3165921835165921836CA7INTERGENICpossibly homozygous72555581
3165921838165921839CT7INTERGENICpossibly homozygous72555584
3165921855165921856GA7INTERGENICpossibly homozygous72555590
3165924253165924254CT17INTERGENIChomozygous72555593
3165936754165936755GA17INTERGENICheterozygous72555604
3165939817165939818GC25INTERGENIChomozygous72555610
3165941415165941416TC14INTERGENIChomozygous72555613
3165957695165957696AC10INTERGENIChomozygous72555619
3165961814165961815TA20INTERGENIChomozygous72555622
3165965314165965315AT10INTERGENICpossibly homozygous72555628
3165965498165965499CT49INTERGENICheterozygous72555631
3165965315165965316AT11INTERGENICpossibly homozygous74072120
3165960567165960568AC12INTERGENIChomozygous79661902
3165960568165960569CA12INTERGENIChomozygous79661904
3165965310165965311AT7INTERGENIChomozygous79661906
3165965311165965312AG7INTERGENIChomozygous79661908
3165967225165967226GT43INTERGENIChomozygous72286925
3165967262165967263CA27INTERGENIChomozygous72286926
3165968775165968776GA27INTERGENICpossibly homozygous72555643