chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3149628748149628749GGAAT2GENIChomozygous698851138
3149629438149629439AG21GENICpossibly homozygous546873454
3149629711149629712TC17GENIChomozygous546873455
3149630403149630404TA20GENIChomozygous546873456
3149630706149630707CT16GENIChomozygous546873457
3149630796149630797CA15GENICpossibly homozygous546873458
3149630816149630817CT15GENICpossibly homozygous546873459
3149630841149630842TC23GENIChomozygous546873460
3149630974149630975TC21GENIChomozygous546873461
3149631037149631038AG18GENICpossibly homozygous546873462
3149631151149631152CT14GENICpossibly homozygous548342131
3149631339149631340AG13GENIChomozygous546873463
3149631435149631436CT22GENIChomozygous546873464
3149631552149631553TC23GENIChomozygous546873465
3149631663149631664TA24GENICpossibly homozygous546873466
3149631723149631724GA19GENICpossibly homozygous546873467
3149632126149632127TC19GENIChomozygous546873468
3149632178149632179GA15GENIChomozygous546873469
3149632226149632227GT14GENICpossibly homozygous548342132