chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117404141074041411GA11GENIChomozygous116355632
117404162974041630GA26GENICpossibly homozygous115990559
117404165674041657TG27GENIChomozygous115990561
117404198574041986CT34GENIChomozygous116355633
117404213074042131TC39GENIChomozygous116355634
117404233874042339CT33GENIChomozygous116355635
117404247674042477CT19GENIChomozygous116355636
117404283974042840TC13GENIChomozygous116054476
117404294274042943GT26GENIChomozygous116355637
117404312774043128AT14GENIChomozygous115990571
117404347974043480CT19GENIChomozygous115990575
117404358074043581GA23GENIChomozygous116355638
117404362174043622TC24GENIChomozygous115990577
117404369774043698GA14GENIChomozygous116355639
117404402874044029TG20GENIChomozygous116355640
117404404174044042TC21GENIChomozygous115990581
117404408874044089AG24GENIChomozygous115990583
117404500374045004GA25GENIChomozygous116277963
117404511674045117AG19GENIChomozygous116355641
117404518974045190GA18GENIChomozygous116277965
117404528974045290AG18GENIChomozygous115990589
117404622874046229AG19GENIChomozygous116355642
117404637674046377GC17GENIChomozygous115990593
117404657674046577AG20GENIChomozygous115990595
117404676774046768CT19GENIChomozygous115990597
117404681374046814GA12GENIChomozygous116277967
117404698974046990CT12GENIChomozygous116277969
117404709674047097CT12GENIChomozygous116054484
117404740974047410GA23GENIChomozygous116355643
117404787274047873CT28GENIChomozygous116355644
117404862874048629CT18GENIChomozygous116277971
117404880674048807CT26GENIChomozygous116277973
117404898174048982TC14GENIChomozygous115990599
117404929374049294GA29GENIChomozygous115990603
117405029274050293AC17GENIChomozygous115990607
117405153474051535CG21GENIChomozygous115990611
117405163674051637GC15GENIChomozygous115990613
117405169574051696CT16GENIChomozygous116277978