chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
62398942123989422CA21GENIChomozygous126347891
62399056423990565GT7GENIChomozygous126347892
62399408223994083CG21GENIChomozygous126347893
62399577523995776TG13GENIChomozygous126347894
62399984123999842AC13GENIChomozygous126347895
62400084424000845CT14GENIChomozygous126347896
62400148824001489TC11GENIChomozygous126347897
62400373124003732GC25GENIChomozygous126347898
62400503424005035GA19GENIChomozygous126347899
62400508024005081TC11GENIChomozygous126347900
62400521524005216GA17GENIChomozygous126347902
62400528024005281CT13GENIChomozygous126347903
62400544524005446AT19GENIChomozygous126347904
62400558224005583AG12GENIChomozygous126347905
62400632024006321TC7GENIChomozygous126347906
62400659924006600GA25GENIChomozygous126347907
62400663024006631TC25GENIChomozygous126347908
62400705024007051GA14GENIChomozygous126347909
62400726624007267AG16GENIChomozygous126347910
62400731624007317TG10GENIChomozygous126347911
62400733224007333CG12GENIChomozygous126347912
62400741324007414CG10GENIChomozygous126347913
62400742424007425AG8GENIChomozygous126347914
62400746024007461GA15GENIChomozygous126347915
62400763424007635TC11GENIChomozygous126347916
62400770424007705TC15GENIChomozygous126347917
62400866324008664AC8GENIChomozygous126347919
62400866624008667GA9GENIChomozygous126347920
62400870324008704AG12GENIChomozygous126347921
62400881024008811GT6GENIChomozygous126347926
62400887824008879GA10GENIChomozygous126347927
62400888424008885AG8GENIChomozygous126347928