chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6122926493122926493T10GENICheterozygous129928841
6122930584122930585TC21GENIChomozygous114974596
6122934436122934437GA17GENIChomozygous114974597
6122939844122939845GA19GENIChomozygous114974598
6122943780122943781AT18GENICpossibly homozygous115080033
6122951862122951863TC18GENIChomozygous114974599
6122961350122961351CT16GENIChomozygous114974600
6122962410122962411CT16GENIChomozygous114974601
6122970954122970955TG28GENIChomozygous114974603
6122943948122943949G19GENIChomozygous128390873
6122960834122960835C18GENIChomozygous128390874