chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45546844155468442TTGTGTGTGTGTGTGTGTGA1GENIChomozygous58334735
45546857955468580AT16GENICpossibly homozygous57727583
45547008555470136TGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGC---------------------------------------------------3GENIChomozygous58334736
45547053955470540AG14GENICpossibly homozygous57727587
45547062155470622TC14GENIChomozygous57727589
45547097855470979CT12GENIChomozygous57727591
45547101855471019TTA1GENIChomozygous57833055
45547110955471110AG19GENIChomozygous57727593
45547141355471414GC14GENIChomozygous57727595
45547162555471626CT31GENIChomozygous57727597
45547171255471713TC19GENICpossibly homozygous57727599
45547194455471945AAT19GENIChomozygous57727601
45547243055472431TC14GENIChomozygous58334739
45547243255472433CT12GENIChomozygous58334740
45547247155472472TTATGA2GENIChomozygous57727605
45547260255472603AG1GENIChomozygous57727609
45547260555472606TC3GENIChomozygous57727611
45547316055473161GA11GENICpossibly homozygous57727615
45547345355473454TA11GENIChomozygous57727617
45547346155473467TTTATT------13GENIChomozygous57727619
45547349055473491CCG13GENIChomozygous57727621
45547350855473509AG10GENIChomozygous57727623
45547358355473584TC20GENICpossibly homozygous57727625
45547377655473777GA21GENICpossibly homozygous57727629
45547417755474178TA22GENIChomozygous57727633
45547468455474685GA12GENIChomozygous57727635
45547541555475416CCAGTCAGTCAGTT2GENICheterozygous58076121
45547541755475418TTGATACTG2GENICheterozygous58076123
45547558955475590CT14GENIChomozygous57727637
45547578755475788GA23GENICpossibly homozygous58076125
45547664255476643TC17GENIChomozygous57727639