chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99441893494418935TA42GENIChomozygous138631061
99441901694419017CT40GENIChomozygous138631062
99441913794419138AG36GENIChomozygous138631063
99441933094419331TG54GENIChomozygous138631064
99441944094419441GA59GENIChomozygous138631065
99441957694419577CT51GENIChomozygous138631066
99441960894419609TC55GENIChomozygous138631067
99442020494420205TC46GENIChomozygous138631068
99442096294420963AG38GENIChomozygous138631069
99442117394421174AG57GENIChomozygous138631070
99442216494422165GT44GENIChomozygous138631071
99442230394422304TC39GENIChomozygous138631072
99442274694422747CG41GENIChomozygous138631073
99442305394423054CT42GENIChomozygous138631074
99442305494423055CT41GENIChomozygous138631075
99442371394423714TA43GENIChomozygous138631076
99442528894425289GA36GENIChomozygous138631077
99442690694426907GA40GENIChomozygous138631078
99442716594427166CT65GENIChomozygous138631079
99442676594426766G36GENICheterozygous403731422
99442676594426766GA36GENIChomozygous403731421
99442311194423112C46GENIChomozygous138474659