chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104024774740247748GC10GENIChomozygous116568879
104024828040248281CG7GENIChomozygous116764008
104024828740248288AG11GENIChomozygous116568883
104024830040248301CT14GENIChomozygous116568885
104024848040248481CA13GENIChomozygous116764010
104024858740248588CG20GENIChomozygous116764012
104024863840248639CT11GENIChomozygous116764014
104024893840248939TC13GENIChomozygous116764016
104024970040249701TC14GENIChomozygous116568889
104024994740249948TG10GENIChomozygous116764020
104025124040251241GA8GENIChomozygous116764022
104025152940251530TC12GENIChomozygous116870428
104025156340251564GC15GENIChomozygous126380860
104025173540251736AG14GENIChomozygous116764024
104025205140252052CT10GENIChomozygous116764026
104025293440252935TC10GENIChomozygous116764030
104025345040253451CT15GENIChomozygous116764034
104025375140253752TC8GENIChomozygous116870430
104025399140253992TC11GENIChomozygous116764036
104025419140254192AC18GENIChomozygous116764038
104025434740254348AG15GENIChomozygous116764040
104025437640254377GA9GENICheterozygous116764042
104025471040254711TC7GENIChomozygous116870432
104025487440254875CT5GENICheterozygous116764046
104025499340254994GA25GENIChomozygous116764048