chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55949076359490764AG24GENIChomozygous935036921
55949103459491035GA11GENIChomozygous935036922
55949225259492253GA25GENIChomozygous935036923
55949329359493294TC22GENIChomozygous935036924
55949334459493345CT21GENIChomozygous935036925
55949402159494022GT17GENIChomozygous935036926
55949502159495022AG24GENIChomozygous935036927
55949624259496243AG27GENIChomozygous935036928
55949666359496664TA12GENICpossibly homozygous935036929
55949727059497271GA26GENIChomozygous935036930
55950017959500180AG33GENIChomozygous935036931
55950082859500829GC27GENIChomozygous935036932
55950087359500874GA33GENIChomozygous935036933
55950087559500876CT34GENIChomozygous935036934
55950220759502208CA22GENIChomozygous935036935
55950224359502244CT18GENIChomozygous935036936
55950230059502301GA24GENIChomozygous935036937
55950234059502341CT25GENIChomozygous935036938
55950246859502469CT29GENIChomozygous935036939
55950268359502684TC18GENIChomozygous935036940
55950269859502699AT25GENIChomozygous935036941
55950323259503233CT14GENIChomozygous935036942
55950324559503246CT9GENIChomozygous935036943
55950345359503454CT15GENIChomozygous935036944
55950351459503515TC21GENIChomozygous935036945
55950372059503721TC26GENICpossibly homozygous935036946
55950448859504489AG16GENIChomozygous935036947
55950488859504889TC19GENIChomozygous935036948
55950514059505141CT14GENIChomozygous935036949
55950546359505464TC23GENIChomozygous935036950
55950571859505719GA14GENIChomozygous935036951
55950586959505870TC25GENICheterozygous935036952