chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46976452469764525TA10GENIChomozygous112697299
46976459969764600GT15GENIChomozygous112697301
46976464969764650AG14GENIChomozygous112697303
46976468569764686TC14GENIChomozygous112697305
46976471669764717TC22GENIChomozygous112697307
46976478969764790TC20GENIChomozygous112697309
46976486369764864GA14GENIChomozygous112697311
46976498469764985TC21GENIChomozygous112697313
46976502269765023CG20GENIChomozygous119277733
46976506069765061AG26GENIChomozygous112697315
46976507469765075CT22GENIChomozygous112697317
46976512569765126AG25GENIChomozygous112697319
46976516469765165GC30GENICpossibly homozygous112697321
46976545369765454GA22GENIChomozygous112697323
46976559569765596CT18GENIChomozygous112697325
46976563669765637CG14GENIChomozygous112697327
46976624669766247TA15GENIChomozygous112697339
46976632269766323GA19GENIChomozygous119277735
46976632369766324AG19GENIChomozygous113275809
46976632669766327TA20GENIChomozygous112697341
46976636969766370CT23GENIChomozygous112697343
46976650769766508AG32GENIChomozygous112697345
46976653469766535CT28GENIChomozygous112697347
46976654469766545GA26GENIChomozygous112697349
46976663769766638AG11GENIChomozygous112697353