chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149183330149183331TG59GENIChomozygous112880540
4149183833149183834GA33GENICheterozygous112880542
4149184196149184197TC60GENIChomozygous112880544
4149184534149184535CT40GENICheterozygous113060141
4149184932149184933CA79GENIChomozygous112880546
4149185296149185297TG75GENIChomozygous112880548
4149185408149185409AG65GENIChomozygous112880550
4149185441149185442CT57GENIChomozygous112880552
4149186124149186125GA66GENIChomozygous112880553
4149186677149186678TC73GENIChomozygous112880555
4149187685149187686CA81GENIChomozygous112880556
4149188291149188292TC25GENIChomozygous112880558
4149190086149190087GA66GENIChomozygous112880560
4149190431149190432GA60GENIChomozygous112880562
4149190469149190470GA67GENIChomozygous112880564
4149190633149190634GC44GENIChomozygous112880566
4149190997149190998GA58GENIChomozygous112880567
4149191157149191158TA48GENICpossibly homozygous112880569
4149191241149191242TC48GENIChomozygous112880571
4149191247149191248CT50GENIChomozygous112880573
4149191382149191383TC58GENIChomozygous112880575
4149191769149191770AG46GENIChomozygous112880577
4149191776149191777TC46GENIChomozygous112880579
4149191802149191803GA52GENIChomozygous112880580
4149191817149191818TC59GENICpossibly homozygous112880582
4149191846149191847AG57GENIChomozygous112880584