chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124547041845470419AG22GENIChomozygous50216397
124547053145470532GA29GENIChomozygous50216398
124547066745470668GGTTTAT13GENIChomozygous50216399
124547070045470701TTAA13GENIChomozygous50216400
124547071345470714GA15GENIChomozygous50216401
124547113445471135TC13GENIChomozygous50216402
124547139145471392TC13GENIChomozygous50216403
124547143545471436TC18GENIChomozygous50386294
124547066445470665GA16GENIChomozygous50386292
124547109845471099GA17GENIChomozygous50386293
124547145345471454TC21GENIChomozygous50216404
124547157645471577GT29GENIChomozygous50216405
124547161745471618AAT19GENIChomozygous50216406
124547177145471773TT--10GENICheterozygous50386295
124547260945472610AT25GENIChomozygous50216409
124547278045472781AAAAGGTAG21GENIChomozygous50216410
124547278145472782CCAAG18GENIChomozygous50216411
124547288345472884CT28GENIChomozygous50386296
124547299245473010GAGACAGGCTGTGGGTGC------------------16GENIChomozygous50386297
124547321745473218AT24GENIChomozygous50386298
124547359245473593CT27GENIChomozygous50216412
124547410445474105GA24GENIChomozygous50386299
124547474745474748TA28GENIChomozygous50216413
124547531045475311GA18GENIChomozygous50216414
124547560245475603GA26GENIChomozygous50216415
124547587845475879TTCATG29GENIChomozygous50216416
124547612545476126GGCA12GENIChomozygous50216418
124547622545476228TTG---17GENIChomozygous50216419
124547636345476364AG31GENIChomozygous50216421
124547637645476377CT29GENIChomozygous50216422
124547662545476626TC35GENIChomozygous50216423
124547681245476813TC24GENIChomozygous50216424
124547689645476897A-22GENIChomozygous50216425
124547690045476901GT21GENIChomozygous50216426
124547692045476921TC26GENIChomozygous50216427
124547735645477359CCG---21GENIChomozygous50216428