chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
371446067144607GA17GENIChomozygous111871766
371447307144731CT21GENIChomozygous111871768
371455267145527AG16GENIChomozygous111871770
371455547145555AT15GENIChomozygous111871772
371455867145587AG18GENIChomozygous111871774
371456357145636TA22GENIChomozygous111871776
371457137145714TC21GENIChomozygous111871778
371457867145787AG29GENIChomozygous111871780
371458347145835CT28GENIChomozygous111871782
371459737145974TC22GENIChomozygous111871784
371462187146219GA23GENIChomozygous111871786
371468037146804AC24GENIChomozygous111871794
371465517146552TC24GENIChomozygous111871788
371466947146695TC25GENICpossibly homozygous111871790
371467687146769CT21GENIChomozygous111871792
371478777147878AG34GENIChomozygous111871796
371479007147901TC31GENIChomozygous111440111
371480477148048AG30GENIChomozygous111871798
371482137148214AC18GENIChomozygous111871800
371484747148475TC12GENIChomozygous111871802
371485447148545CT27GENIChomozygous111871804
371486187148619TC22GENIChomozygous111871806
371486307148631AG21GENIChomozygous111871808
371487497148750CT28GENIChomozygous111871811
371494557149456GA19GENIChomozygous111871813
371497277149728CT19GENIChomozygous111871815
371500787150079AG32GENICpossibly homozygous111871817
371501027150103AG31GENICpossibly homozygous111440113
371501657150166AT28GENIChomozygous111871819
371535737153574GA24GENIChomozygous111871825
371538147153815GT31GENIChomozygous111871827
371540307154031CT24GENICpossibly homozygous111871829
371542327154233TC13GENIChomozygous111440115
371603527160353TC30GENIChomozygous111440126
371627527162753TA24GENIChomozygous111440130