chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75888884658888847AC11GENIChomozygous54856310
75888965758889658CA10GENICpossibly homozygous54856311
75888996758889968TTG10GENIChomozygous54856312
75889003258890033CT14GENIChomozygous55568163
75889096758890968CT8GENIChomozygous54856315
75889163258891633CT19GENIChomozygous54856316
75889177658891777TC13GENIChomozygous54856317
75889193758891938CT9GENICheterozygous54856318
75889193858891939AG9GENICheterozygous54856319
75889209458892095CT9GENICpossibly homozygous55568165
75889223358892234GA13GENICpossibly homozygous54856320
75889234258892346GTAA----7GENIChomozygous54856321
75889242058892421CT6GENIChomozygous54856322
75889252758892528CT6GENIChomozygous54856323
75889270858892709CG14GENIChomozygous54856324
75889279758892800ATT---5GENICheterozygous54856325
75889291058892911GC11GENIChomozygous54856326
75889300558893006GA8GENIChomozygous55568167
75889305558893065TTTTTTTCTT----------3GENICheterozygous54856327
75889307358893074GC4GENIChomozygous54856328
75889323058893231AG14GENICpossibly homozygous54856329
75889331158893312TC14GENIChomozygous54856330
75889394458893945CT11GENIChomozygous54856331
75889397858893979GA10GENICheterozygous54856332
75889403658894037GA16GENICpossibly homozygous54856333