chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117404141074041411GA49GENIChomozygous116355632
117404162974041630GA28GENIChomozygous115990559
117404165674041657TG31GENIChomozygous115990561
117404198574041986CT74GENIChomozygous116355633
117404213074042131TC51GENIChomozygous116355634
117404233874042339CT40GENIChomozygous116355635
117404247674042477CT48GENICpossibly homozygous116355636
117404283974042840TC51GENIChomozygous116054476
117404294274042943GT57GENIChomozygous116355637
117404312774043128AT28GENIChomozygous115990571
117404347974043480CT26GENIChomozygous115990575
117404358074043581GA44GENIChomozygous116355638
117404362174043622TC51GENIChomozygous115990577
117404369774043698GA49GENIChomozygous116355639
117404402874044029TG48GENIChomozygous116355640
117404404174044042TC50GENIChomozygous115990581
117404408874044089AG46GENIChomozygous115990583
117404528974045290AG32GENIChomozygous115990589
117404500374045004GA28GENIChomozygous116277963
117404511674045117AG36GENIChomozygous116355641
117404518974045190GA28GENIChomozygous116277965
117404622874046229AG48GENIChomozygous116355642
117404676774046768CT49GENIChomozygous115990597
117404681374046814GA48GENIChomozygous116277967
117404698974046990CT57GENIChomozygous116277969
117404709674047097CT57GENIChomozygous116054484
117404740974047410GA28GENIChomozygous116355643
117404787274047873CT43GENIChomozygous116355644
117404862874048629CT53GENIChomozygous116277971
117404880674048807CT61GENIChomozygous116277973
117404898174048982TC45GENIChomozygous115990599
117404910874049109CT23GENIChomozygous115990601
117404929374049294GA20GENIChomozygous115990603
117405029274050293AC45GENIChomozygous115990607
117405153474051535CG52GENIChomozygous115990611
117405163674051637GC68GENIChomozygous115990613
117405169574051696CT62GENIChomozygous116277978