chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120718785120718786TTC34GENIChomozygous54084775
7120718786120718787AT32GENIChomozygous54921130
7120719529120719530CT48GENIChomozygous54084776
7120719582120719589CTGAGCT-------40GENIChomozygous54084777
7120719913120719914TC30GENIChomozygous54084778
7120720004120720005CCA44GENIChomozygous54084779
7120720195120720199AGGA----28GENIChomozygous54084780
7120723225120723226G-4GENIChomozygous54084788
7120725519120725520TA37GENIChomozygous54084789
7120725762120725763TG32GENIChomozygous54084790
7120726710120726711TC58GENIChomozygous54084791
7120728835120728836CCTGTGTGTGTGTGTGTGTGTG6GENICheterozygous55001836
7120728835120728836CCTGTGTGTGTGTG6GENICheterozygous55096200
7120729949120729950AAG19GENIChomozygous54084793
7120732604120732605AC21GENIChomozygous54084795
7120733097120733107TGTGTGTGTG----------32GENICheterozygous55096202
7120733099120733107TGTGTGTG--------32GENICpossibly homozygous55096204
7120733141120733142AC41GENIChomozygous54084797
7120734255120734256CCGTGTGTGTGT9GENICpossibly homozygous55096206
7120734255120734256CCGTGTGT9GENICheterozygous55144778
7120734506120734507GA43GENIChomozygous54084798
7120734925120734927GT--4GENICheterozygous55361861
7120735166120735167CT38GENIChomozygous54084799
7120735185120735186GA40GENIChomozygous54084800
7120735677120735678G-30GENICheterozygous55144779
7120735693120735694G-15GENICheterozygous54921132
7120735693120735698GAGAG-----15GENICheterozygous55059675
7120735695120735700GAGAG-----16GENICheterozygous54084802
7120738000120738001CCCCT17GENIChomozygous54084805