chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108534544685345447C17GENICheterozygous144857386
108534757885347578CAGGGTTTCTCTTGTAG44GENIChomozygous144857387
108534772285347723GA48GENICpossibly homozygous144873010
108534773185347732TC49GENICpossibly homozygous144873011
108534782485347825CT39GENIChomozygous144873012
108534819885348199CA40GENIChomozygous144873013
108534821185348212GA41GENIChomozygous144873014
108534865485348655AG40GENIChomozygous144873015
108534897685348977AG30GENIChomozygous144873016
108534924285349246TACA35GENIChomozygous144857388
108534929985349300CT25GENIChomozygous144873017
108534939285349393CA27GENIChomozygous144873018
108534964285349643AG42GENIChomozygous143462936
108534980385349804TC47GENIChomozygous144873019
108534980685349808CA47GENIChomozygous144857389
108534988285349883TC38GENIChomozygous144873020
108534991285349913CG40GENIChomozygous143462938
108534991485349915CT39GENIChomozygous144873021
108535004285350043AT16GENIChomozygous144873022
108535006985350079ATGTAATAAA12GENIChomozygous144857390
108535008285350111ATAAATCTTTTTAAAAAAATCTCTCTGGG12GENIChomozygous144857391
108535022585350229AGAA29GENIChomozygous144857392
108535034885350349TC41GENIChomozygous144873023
108535293985352940TC30GENIChomozygous144873024
108535295685352959TTG22GENICpossibly homozygous144857393
108535297385352973T26GENIChomozygous144857394
108535305185353052AG38GENIChomozygous144873025
108535343185353431TGTGTATGTATGTGTGTGTATGTGTGTGTA20GENICpossibly homozygous144857396
108535346285353463CG23GENIChomozygous144873026
108535455585354556AT57GENIChomozygous143462942
108535458385354584GA52GENIChomozygous144873027
108535688485356885CT50GENIChomozygous144873028
108535708285357083CT51GENIChomozygous144873029
108535741885357419GA46GENIChomozygous144873030