chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
166848677368486774AG32GENIChomozygous47509055
166848697968486980AC23GENIChomozygous47509056
166848756668487567AG19GENIChomozygous47509057
166848798068487981TTAAA6GENICheterozygous47509060
166848800168488002GA14GENICheterozygous47509061
166848801168488020CACAGGCAG---------6GENIChomozygous47509062
166848986168489862GT15GENIChomozygous47509063
166849020268490203TA16GENIChomozygous47509064
166849046568490466AG15GENIChomozygous47509065
166849068368490684CA18GENIChomozygous47771663
166849068668490687CA18GENIChomozygous47509066
166849092568490926AG28GENIChomozygous47509067
166849161168491612GA39GENIChomozygous47509068
166849177968491780GA26GENIChomozygous47509069
166849192468491925AG22GENIChomozygous47509070
166849198268491983CA25GENIChomozygous47771664
166849210268492103CT30GENIChomozygous47509071
166849224168492242AG21GENIChomozygous47509072
166849229768492298A-10GENIChomozygous47509073
166849235668492357CT13GENICheterozygous47509074
166849261468492615CT18GENIChomozygous47771665
166849281468492815GA19GENIChomozygous47771666
166849289668492897CCT16GENIChomozygous47771667
166849290068492901TC18GENICpossibly homozygous47771668
166849296268492963AAT20GENIChomozygous47509076
166849302468493025CA21GENIChomozygous47771669
166849317168493172GA31GENIChomozygous47771670
166849322768493228TC19GENIChomozygous47509081
166849324868493249AATGTTG21GENIChomozygous47509082