chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103470469034704691GA33GENIChomozygous116924569
103470499234704993GA25GENIChomozygous116924571
103470534434705345AG18GENIChomozygous116556334
103470540334705404AC16GENIChomozygous116556336
103470543334705434AG16GENIChomozygous116757025
103470549934705500GA19GENIChomozygous116556338
103470556134705562CG16GENIChomozygous116556340
103470717734707178CT24GENIChomozygous116556342
103470833234708333GA27GENIChomozygous116556344
103470854134708542TG24GENIChomozygous116556346
103470932534709326CA24GENIChomozygous116757029
103470942534709426CT28GENIChomozygous116556352
103470971234709713GA19GENIChomozygous116556356
103471149134711492GA17GENIChomozygous116757039
103471152134711522TA21GENIChomozygous116556370
103471152334711524AG21GENIChomozygous116556372
103471166434711665GT34GENIChomozygous116924573
103471170334711704TC33GENIChomozygous116924575
103471174834711749CT40GENIChomozygous116556374
103471179034711791AG31GENIChomozygous116556376
103471185634711857TA29GENIChomozygous116556378
103471186934711870AT29GENIChomozygous116556380
103471189334711894GA33GENIChomozygous116556382
103471209134712092TA21GENIChomozygous116556384
103471215534712156AG22GENIChomozygous116556386
103471450034714501GA24GENIChomozygous116556392
103471455134714552AG22GENIChomozygous116556394
103471668734716688CT20GENIChomozygous116924577
103472661034726611TC22GENIChomozygous116924579
103472716734727168GT24GENIChomozygous116556400