chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97481733274817333GGA2GENICheterozygous53143994
97482018374820187AGAG----1GENIChomozygous53143997
97483560374835604A-20GENIChomozygous52022531
97484588574845886TTTCTATCTA10GENICpossibly homozygous53481030
97485520774855208CA18GENIChomozygous52022615
97486421474864215AC13GENIChomozygous53481031
97488723474887235AAAG5GENICheterozygous52911191
97488723474887235AAAGAGAGAGAGAGAGAGAG5GENICheterozygous52911193
97490227374902274AAAC6GENICheterozygous52022960
97491305674913057CCAG3GENICheterozygous52911196
97491305674913057CCAGAGAGAGAGAG3GENICheterozygous52911197
97491829674918297T-19GENICheterozygous52857181
97492679774926798T-22GENIChomozygous52023227
97492680074926801T-21GENIChomozygous52023229
97492941074929411TTAC18GENICheterozygous52023256
97492941974929421AC--18GENICheterozygous52911201
97493912574939127TG--13GENICheterozygous52951621
97497349874973499CA10GENIChomozygous52023458
97501560375015604T-4GENICheterozygous52236713
97501648375016484AATGTG4GENIChomozygous52023597
97502510775025108GGCT7GENICheterozygous52236749
97504460075044602CT--7GENICheterozygous52911213
97504963875049640AT--4GENICheterozygous52024010
97502453275024534AG--6GENIChomozygous52558675
97508106075081064TCTA----3GENIChomozygous53296937
97510536575105366CG19GENIChomozygous52024367
97511002075110022GT--10GENICheterozygous52024388
97512302475123025A-14GENIChomozygous52024390
97512887875128880TC--3GENICheterozygous52911219
97517407075174071C-4GENIChomozygous53209958
97518624175186242AT17GENIChomozygous52024424
97518624275186243TTC17GENIChomozygous52024426
97520375475203756AC--2GENICheterozygous53296939
97524425975244261TA--1GENIChomozygous52024432
97525704075257041A-5GENICheterozygous52473189
97527291775272918TG8GENICheterozygous52238275
97527292175272922CT8GENICheterozygous52238277
97527799975278000GGCT10GENICheterozygous52024438
97529280675292808CA--7GENICheterozygous52988506
97530501475305015A-13GENIChomozygous52024442