chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103930109839301099CA32GENIChomozygous944625941
103930810739308108AG29GENIChomozygous944625942
103930815839308159TA27GENIChomozygous944625943
103930816639308167CT25GENIChomozygous944625944
103930907239309073GA25GENIChomozygous944625945
103931007039310071TC25GENIChomozygous944625946
103931188339311884GA11GENIChomozygous944625947
103931405139314052TC16GENIChomozygous944625948
103931458139314582AG27GENIChomozygous944625949
103931563739315638CT32GENIChomozygous944625950
103931601239316013TC35GENIChomozygous944625951
103931697739316978CT44GENIChomozygous944625952
103931718139317182AC35GENIChomozygous944625953
103931745639317457GA40GENIChomozygous944625954
103931766839317669AC31GENIChomozygous944625955
103931782539317826AT25GENIChomozygous944625956
103931893939318940GA31GENIChomozygous944625957
103931974439319745TC30GENIChomozygous944625958
103932098639320987GA29GENIChomozygous944625959
103932099939321000GA35GENIChomozygous944625960
103932129639321297AG32GENIChomozygous944625961
103932137539321376CA32GENIChomozygous944625962
103932142339321424TC24GENIChomozygous944625963
103932144539321446TG27GENIChomozygous944625964
103932168039321681AC43GENIChomozygous944625965
103932211239322113AG27GENIChomozygous944625966
103932222539322226CT21GENIChomozygous944625967
103932251339322514GC30GENIChomozygous944625968
103932319339323194GA28GENIChomozygous944625969
103932387439323875TC13GENIChomozygous944625970
103932389339323894AT13GENIChomozygous944625971
103932403839324039GA18GENIChomozygous944625972
103932416239324163TA28GENIChomozygous944625973
103932431539324316CT25GENIChomozygous944625974