chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1811431241143125GT88GENIChomozygous110568909
1811457541145755CT55GENIChomozygous110568911
1811477591147760TC66GENIChomozygous110568913
1811492351149236GA55GENIChomozygous110512408
1811502121150213GA55GENIChomozygous119577900
1811502141150215AT55GENIChomozygous119509952
1811502151150216AG55GENIChomozygous119577901
1811502231150224TC52GENIChomozygous119509954
1811502441150245GT45GENIChomozygous119509956
1811507411150742CT55GENIChomozygous110568915
1811510281151029AG70GENIChomozygous110568917
1811511621151163TC52GENIChomozygous110568920
1811518001151801TC68GENIChomozygous110568922
1811518181151819TC71GENIChomozygous110568925
1811519621151963AG64GENIChomozygous110568927
1811531121153113AG45GENIChomozygous110640989
1811540811154082CT50GENIChomozygous110512410
1811541971154198GA61GENIChomozygous110568930
1811577711157772AC49GENICpossibly homozygous110512415
1811532231153223TAATCT37GENIChomozygous131202381
1811550321155033T43GENIChomozygous131202382
1811599241159925CT46GENIChomozygous110512419
1811612741161275GA64GENIChomozygous110512422
1811626741162675GA60GENIChomozygous110568932
1811642541164255TA56GENIChomozygous110568935
1811662901166291GA40GENIChomozygous110512426
1811665731166574TC69GENIChomozygous119509958
1811668301166831TC64GENIChomozygous119509966
1811682841168285GT69GENIChomozygous110512428
1811702811170282GA50GENIChomozygous110568937
1811704901170491TG53GENIChomozygous110512430
1811718141171815GA47GENIChomozygous110568940
1811718941171895GA40GENIChomozygous110568942
1811726371172638GA68GENIChomozygous110512432
1811752231175223TTTCAGA54GENIChomozygous131202386
1811666291166630CG66GENIChomozygous119542371
1811649251164948TGCGTCCTCTTCCCCACTGAGTA56GENIChomozygous132754610