chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48485543184855432GC13GENIChomozygous113129644
48485546484855465GA14GENIChomozygous119308859
48485666284856663GC30GENIChomozygous112758438
48485704784857048GA28GENIChomozygous112758440
48485705684857057CT27GENIChomozygous112758442
48485707884857079GA21GENIChomozygous113278609
48485724284857243AC24GENIChomozygous113278611
48485755584857556GA30GENIChomozygous112758448
48485778484857785TC16GENIChomozygous112758450
48485792884857929CT18GENIChomozygous119308861
48485834984858350CT24GENIChomozygous119308863
48485845984858460GT24GENIChomozygous119308865
48485911684859117GT30GENIChomozygous112758462
48486001684860017CT32GENIChomozygous119308867
48486467484864675AG26GENIChomozygous112758522
48486539184865392CT18GENIChomozygous119308869
48486581284865813TC30GENIChomozygous119308871
48486735984867360AG32GENIChomozygous112758544
48486747184867472TC25GENIChomozygous112758548
48486755384867554AG33GENIChomozygous112758552
48486770784867708TC27GENIChomozygous112758554
48486858384868584CT27GENIChomozygous119308873
48487063084870631TA22GENIChomozygous119308875
48487123184871232CT17GENIChomozygous113278616
48487124684871247GA17GENIChomozygous113278618
48487146384871464GC23GENIChomozygous113278619
48487339584873396AG29GENIChomozygous112758569
48487510484875105AG22GENIChomozygous112758577