chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97702956877029569TA3GENICheterozygous877770332
97709519777095198AG11GENICheterozygous877770333
97709521977095220AG10GENICheterozygous877770334
97709528877095289AG8GENICheterozygous877770335
97709532677095327CA15GENICheterozygous877770336
97710716577107166TA3GENICheterozygous877770337
97711509977115100TA3GENICheterozygous877770338
97714032177140322AT5GENICheterozygous877770339
97714130577141306GT8GENICheterozygous877770340
97714202977142030CA3GENICheterozygous877770341
97715375377153754TG16GENIChomozygous877770342
97727546277275463AT6GENICheterozygous877770343
97727839277278393TC15GENICheterozygous877770344
97740595077405951AG5GENIChomozygous877770345
97741812277418123CT8GENIChomozygous877770346
97741817277418173CA10GENIChomozygous877770347
97741821077418211CT7GENIChomozygous877770348
97741822077418221GA7GENIChomozygous877770349
97747437477474375AC4GENICheterozygous877770350
97747439977474400TG8GENICheterozygous877770351
97747441877474419GA6GENICheterozygous877770352
97752452477524525CG6GENICheterozygous877770353
97760268077602681GT4GENIChomozygous877770354
97760268177602682AG4GENIChomozygous877770355
97761250677612507CT19GENIChomozygous877770356
97761537777615378CT6GENIChomozygous877770357
97767893277678933AG4GENICheterozygous877784117
97769777177697772CA4GENIChomozygous877770358
97771294777712948AT7GENIChomozygous877770359
97775085877750859CA13GENIChomozygous877770360
97775089877750899CA11GENIChomozygous877770361
97775104777751048TC6GENIChomozygous877770362