chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
63388557733885578AC13GENIChomozygous134423945
63388611933886120AC11GENICheterozygous134485796
63388676633886767G13GENIChomozygous134422134
63388769033887693TGG8GENIChomozygous134422135
63388938933889390GA16GENIChomozygous118657656
63388729133887292CT19GENIChomozygous118657653
63388740333887404AG19GENIChomozygous118657654
63388870233888703CT7GENIChomozygous118657655
63388941033889411AG15GENIChomozygous118657657
63388953033889531GA12GENIChomozygous122666159
63388954733889548TC11GENIChomozygous118657658
63389074033890741AG16GENIChomozygous118657660
63389088733890897GTAGAGTTTT13GENIChomozygous134422136
63389101833891019GA13GENIChomozygous118657661
63389280633892807GA7GENIChomozygous118657664
63389294733892948CT16GENIChomozygous122666161
63389466633894667CT20GENIChomozygous122666162
63389644633896447GT13GENIChomozygous122666163
63389678833896789GA15GENIChomozygous122666164
63389839533898396CA18GENIChomozygous122666165
63390009433900095GA14GENIChomozygous122666167
63390019433900196TA15GENIChomozygous134422137
63390042133900422CT11GENIChomozygous118657668
63390054033900541AC19GENIChomozygous122666169
63390105033901051GA12GENIChomozygous122666170
63390207433902075C4GENIChomozygous130556170
63390394933903950CT10GENIChomozygous134423946
63390408933904090AG17GENIChomozygous118657673
63390548033905481TC18GENIChomozygous126429623
63389772433897725CT16GENIChomozygous126429617
63390389733903898AG16GENIChomozygous126429619
63390711733907118TC20GENICpossibly homozygous118657676
63390757133907572TG12GENIChomozygous118657677
63390780233907803GA25GENIChomozygous118657678