chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103470469034704691GA13GENIChomozygous116924569
103470499234704993GA17GENIChomozygous116924571
103470534434705345AG6GENIChomozygous116556334
103470543334705434AG13GENIChomozygous116757025
103470549934705500GA15GENIChomozygous116556338
103470556134705562CG29GENIChomozygous116556340
103470833234708333GA26GENIChomozygous116556344
103470932534709326CA30GENIChomozygous116757029
103470942534709426CT13GENIChomozygous116556352
103470962334709624GA19GENIChomozygous116556354
103470971234709713GA15GENIChomozygous116556356
103471075034710751CT16GENIChomozygous116757031
103471075834710759CA17GENIChomozygous116757033
103471152134711522TA27GENIChomozygous116556370
103471152334711524AG27GENIChomozygous116556372
103471174834711749CT18GENIChomozygous116556374
103471179034711791AG24GENIChomozygous116556376
103471185634711857TA35GENIChomozygous116556378
103471186934711870AT36GENIChomozygous116556380
103471189334711894GA37GENIChomozygous116556382
103471209134712092TA30GENIChomozygous116556384
103471215534712156AG30GENIChomozygous116556386
103471450034714501GA38GENIChomozygous116556392
103471455134714552AG19GENIChomozygous116556394
103471668734716688CT26GENIChomozygous116924577
103472661034726611TC22GENIChomozygous116924579
103472716734727168GT20GENIChomozygous116556400