chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108156465781564658GA8GENIChomozygous116657223
108156581281565813GA31GENIChomozygous116811855
108156647281566473CG15GENIChomozygous116657225
108156726781567268CA17GENIChomozygous116657227
108156780581567806AG32GENIChomozygous116657229
108157106881571069TC19GENIChomozygous116657233
108157178581571786AG17GENIChomozygous116657235
108157239681572397CT10GENIChomozygous116657237
108157409081574091GT6GENIChomozygous116657239
108157443281574433GT5GENIChomozygous116657241
108157686281576863GA7GENIChomozygous116811857
108157708781577088TA7GENIChomozygous116657243
108157881081578811TC23GENIChomozygous116657247
108157962081579621CT19GENIChomozygous116657249
108157984581579846CT21GENIChomozygous116657251
108158002581580026GA15GENIChomozygous116811861
108158014481580145CT23GENIChomozygous116657253
108158033581580336GA22GENIChomozygous116657255
108158036181580362TC22GENIChomozygous116657257
108158114781581148AG14GENIChomozygous116657261
108158204081582041AT16GENIChomozygous116657263
108158281781582818CT20GENIChomozygous116811863
108158347381583474AG19GENICpossibly homozygous116657267
108158378981583790TC19GENIChomozygous116657269
108158453181584532AG9GENIChomozygous116657271
108158515481585155CT8GENIChomozygous116657273
108158724981587250GA18GENIChomozygous116811865