chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84789351847893519CA22GENIChomozygous660544100
84789391847893919CCTTCCTTCT9GENIChomozygous763347456
84789403347894034TG24GENIChomozygous660544101
84789429647894297CCAGATAGATAGAT8GENIChomozygous763347457
84789434747894348AG31GENIChomozygous660544102
84789456847894573AAAAG-----10GENIChomozygous763347460
84789478147894782AAAGGACATTCTTTTTTTTTTTTTTTTTTGGGTTCTTTTTTTCGGAGCTGGGGATCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC14GENICheterozygous763347461
84789511247895113CA31GENIChomozygous660544103
84789618347896184TA44GENIChomozygous660544104
84789636947896370CCTCCTTCCTTCCT2GENIChomozygous763347462
84789650747896508GT21GENIChomozygous660544105
84789693847896940TT--8GENICheterozygous763347466
84789693947896951TTGTGTGTGTGT------------9GENICheterozygous763347464
84789726847897269GC23GENIChomozygous660544106
84789743247897433AG33GENIChomozygous660544107
84789758647897587CCTTCCTCCCTCCT12GENIChomozygous763347467
84789761447897615CCT11GENIChomozygous763347468
84789767947897680TC12GENIChomozygous660544108
84789771147897712CCTCTTTCTTTCTTTCTT4GENIChomozygous763347471
84789777547897776CCTTCCTTCT4GENIChomozygous763347473
84789816647898170GTGT----23GENICpossibly homozygous763347475
84789817847898182TGTG----18GENICheterozygous763347479
84789870947898710CT27GENIChomozygous660544109
84789873047898731CT28GENIChomozygous660544110
84789879447898795GA19GENIChomozygous660544111
84789881047898811AACCCAGCCG3GENICheterozygous763347480