chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7110485585110485586TC14GENIChomozygous138181278
7110485616110485617GA12GENIChomozygous138181279
7110485690110485691AG5GENIChomozygous138181280
7110486611110486612G14GENIChomozygous137974063
7110486624110486625GA15GENIChomozygous138181282
7110486649110486650AG18GENIChomozygous138181283
7110486668110486669C14GENIChomozygous137974064
7110486955110486961TTTTTT3GENIChomozygous137974065
7110487056110487062TTTCTC15GENIChomozygous137974066
7110487605110487606GA14GENIChomozygous138181288
7110486972110486973AC7GENIChomozygous138181284
7110487097110487098CT17GENIChomozygous138181285
7110487116110487117TC16GENIChomozygous138181286
7110487287110487288GA10GENIChomozygous138181287
7110486738110486739TG12GENIChomozygous143365169
7110486803110486804CG3GENIChomozygous143365170
7110487835110487836TC8GENIChomozygous138181289
7110487871110487872TC10GENIChomozygous138181290
7110487940110487941GA12GENIChomozygous138181291
7110487978110487979CG16GENIChomozygous138181292
7110488001110488002CT16GENIChomozygous138181293
7110488043110488044TA12GENIChomozygous138181294