chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7126456553126456553G44GENIChomozygous128516586
7126457069126457069GGGGA20GENIChomozygous128516587
7126457082126457082G17GENIChomozygous128516588
7126457140126457140C15GENIChomozygous128516589
7126457169126457169C24GENIChomozygous128516590
7126457175126457175C24GENIChomozygous128516591
7126457192126457192G27GENIChomozygous128516592
7126465583126465583G12GENIChomozygous128516595
7126465596126465596T13GENIChomozygous128516596
7126465608126465609T13GENIChomozygous128516597
7126465621126465622G10GENIChomozygous129939370
7126465640126465641T16GENIChomozygous128516598
7126465646126465647G14GENIChomozygous128516599
7126465660126465661G17GENIChomozygous128516600
7126465663126465664G18GENIChomozygous128516601
7126465676126465677G20GENIChomozygous128516602
7126465682126465684GC20GENIChomozygous128516603
7126465688126465689GA20GENIChomozygous115873571
7126465692126465693G22GENICpossibly homozygous128516604
7126465711126465712C23GENIChomozygous128516605