chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46976391569763916TA1GENIChomozygous112697281
46976393569763936CT3GENIChomozygous112697283
46976399169763992CT4GENIChomozygous112697285
46976408269764083CT6GENIChomozygous112697287
46976418269764183GC9GENIChomozygous112697289
46976437269764373AG12GENIChomozygous112697291
46976441069764411AG13GENIChomozygous112697293
46976442969764430TA18GENIChomozygous112697295
46976447269764473AG16GENIChomozygous112697297
46976452469764525TA14GENIChomozygous112697299
46976459969764600GT8GENIChomozygous112697301
46976464969764650AG10GENIChomozygous112697303
46976468569764686TC11GENIChomozygous112697305
46976471669764717TC11GENIChomozygous112697307
46976478969764790TC11GENIChomozygous112697309
46976486369764864GA10GENIChomozygous112697311
46976498469764985TC10GENIChomozygous112697313
46976506069765061AG18GENIChomozygous112697315
46976507469765075CT19GENIChomozygous112697317
46976512569765126AG16GENIChomozygous112697319
46976516469765165GC16GENIChomozygous112697321
46976545369765454GA6GENIChomozygous112697323
46976559569765596CT12GENIChomozygous112697325
46976563669765637CG14GENIChomozygous112697327
46976592969765930CT5GENIChomozygous112697331
46976624669766247TA6GENIChomozygous112697339
46976632669766327TA4GENIChomozygous112697341
46976636969766370CT5GENIChomozygous112697343
46976650769766508AG6GENIChomozygous112697345
46976653469766535CT4GENIChomozygous112697347
46976654469766545GA3GENIChomozygous112697349
46976655469766555TG3GENIChomozygous112697351
46976663769766638AG1GENIChomozygous112697353
46976502269765022A14GENIChomozygous128046438
46976435169764351A14GENIChomozygous128046435
46976442369764423G17GENIChomozygous128046436
46976490369764904G6GENIChomozygous128046437
46976502269765023CG14GENIChomozygous119277733
46976632269766323GA4GENIChomozygous119277735
46976596969765970CA6GENICheterozygous119340132
46976632369766324AG4GENIChomozygous113275809