chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103470499234704993GA20GENIChomozygous116924571
103470534434705345AG33GENIChomozygous116556334
103470540334705404AC40GENIChomozygous116556336
103470543334705434AG39GENIChomozygous116757025
103470549934705500GA43GENIChomozygous116556338
103470556134705562CG47GENIChomozygous116556340
103470717734707178CT11GENIChomozygous116556342
103470854134708542TG40GENIChomozygous116556346
103470860834708609TG17GENIChomozygous117277615
103470932534709326CA16GENIChomozygous116757029
103470942534709426CT35GENIChomozygous116556352
103470962334709624GA14GENIChomozygous116556354
103470971234709713GA24GENIChomozygous116556356
103471043534710436CT18GENIChomozygous116556364
103471067434710675TG26GENIChomozygous116556368
103471075034710751CT34GENIChomozygous116757031
103471075834710759CA38GENIChomozygous116757033
103471078234710783GA44GENIChomozygous116757035
103471078934710790GT47GENIChomozygous116757037
103471080334710804TC52GENIChomozygous117193971
103471080634710807CA50GENIChomozygous117193972
103471149134711492GA13GENIChomozygous116757039
103471152134711522TA13GENIChomozygous116556370
103471152334711524AG14GENIChomozygous116556372
103471166434711665GT21GENIChomozygous116924573
103471170334711704TC28GENIChomozygous116924575
103471174834711749CT22GENIChomozygous116556374
103471179034711791AG16GENIChomozygous116556376
103471185634711857TA14GENIChomozygous116556378
103471186934711870AT15GENIChomozygous116556380
103471189334711894GA15GENIChomozygous116556382
103471209134712092TA26GENIChomozygous116556384
103471215534712156AG27GENIChomozygous116556386
103471450034714501GA15GENIChomozygous116556392
103471455134714552AG21GENIChomozygous116556394
103471668734716688CT42GENIChomozygous116924577
103472661034726611TC29GENIChomozygous116924579
103472716734727168GT67GENIChomozygous116556400