chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207318137207318138CCAGG3GENIChomozygous59355306
2207318378207318379A-9GENIChomozygous59355307
2207318392207318393GA8GENIChomozygous62202863
2207319310207319318AGATAGAT--------21GENIChomozygous60339762
2207320834207320835CA11GENIChomozygous62202865
2207322847207322848C-41GENIChomozygous60158493
2207323162207323163CT27GENIChomozygous60158494
2207323258207323259CG19GENIChomozygous62202867
2207323367207323368TA22GENIChomozygous59355311
2207323379207323380CT25GENICpossibly homozygous62202869
2207323547207323548TC18GENIChomozygous59355313
2207324210207324211GA22GENIChomozygous60158495
2207324415207324416TC25GENIChomozygous60158496
2207324603207324604G-26GENIChomozygous60158497
2207326456207326457AG16GENIChomozygous59355316
2207326928207326929CT11GENIChomozygous62202871
2207327451207327452AG20GENIChomozygous62202873
2207329278207329294CACACACACACACACC----------------5GENICheterozygous62202875
2207330547207330548A-19GENICpossibly homozygous60561224
2207331142207331143GA24GENIChomozygous62202877
2207331459207331460AG21GENIChomozygous59355324
2207331677207331678CCGGAA15GENIChomozygous62202879
2207332394207332397CTC---35GENIChomozygous62202881
2207332944207332945TA22GENIChomozygous59355326