chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149183330149183331TG59GENIChomozygous112880540
4149183833149183834GA34GENIChomozygous112880542
4149184196149184197TC32GENIChomozygous112880544
4149184532149184533CT51GENICheterozygous113562918
4149184932149184933CA49GENIChomozygous112880546
4149185296149185297TG37GENIChomozygous112880548
4149185408149185409AG55GENICpossibly homozygous112880550
4149185441149185442CT66GENIChomozygous112880552
4149186124149186125GA34GENIChomozygous112880553
4149186677149186678TC67GENIChomozygous112880555
4149187685149187686CA50GENIChomozygous112880556
4149188291149188292TC34GENIChomozygous112880558
4149190086149190087GA52GENIChomozygous112880560
4149190431149190432GA43GENIChomozygous112880562
4149190469149190470GA41GENIChomozygous112880564
4149190633149190634GC38GENIChomozygous112880566
4149190997149190998GA15GENIChomozygous112880567
4149191157149191158TA56GENICpossibly homozygous112880569
4149191241149191242TC52GENICpossibly homozygous112880571
4149191247149191248CT53GENICpossibly homozygous112880573
4149191382149191383TC64GENIChomozygous112880575
4149191769149191770AG40GENIChomozygous112880577
4149191776149191777TC41GENIChomozygous112880579
4149191802149191803GA52GENICpossibly homozygous112880580
4149191817149191818TC45GENIChomozygous112880582
4149191846149191847AG48GENIChomozygous112880584