chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84789351847893519CA15GENIChomozygous573963454
84789391847893919CCTTCCTTCT12GENIChomozygous714617100
84789403347894034TG18GENIChomozygous573963455
84789429647894297CCAGATAGATAGAT3GENIChomozygous714617101
84789434747894348AG8GENIChomozygous573963456
84789456847894573AAAAG-----13GENIChomozygous714617104
84789478147894782AAAGGACATTCTTTTTTTTTTTTTTTTTTGGGTTCTTTTTTTCGGAGCTGGGGATCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC17GENICheterozygous714617105
84789511247895113CA39GENIChomozygous573963457
84789618347896184TA23GENIChomozygous573963458
84789636947896370CCTCCTTCCTTCCT7GENIChomozygous714617106
84789650747896508GT32GENIChomozygous573963459
84789693847896940TT--12GENICheterozygous714617110
84789693947896949TTGTGTGTGT----------18GENICheterozygous714617109
84789726847897269GC42GENIChomozygous573963460
84789743247897433AG36GENIChomozygous573963461
84789761447897615CCT15GENIChomozygous714617111
84789767947897680TC18GENIChomozygous573963462
84789771147897712CCTCTTTCTTTCTTTCTTTCTT11GENIChomozygous714617115
84789777547897776CCTTCCTTCT14GENIChomozygous714617116
84789816647898170GTGT----23GENICheterozygous714617118
84789816847898170GT--23GENICheterozygous714617119
84789817647898182TGTGTG------30GENICheterozygous714617121
84789817847898182TGTG----30GENICheterozygous714617122
84789870947898710CT18GENIChomozygous573963463
84789873047898731CT18GENIChomozygous573963464
84789879447898795GA21GENIChomozygous573963465
84789881047898811AACCCAGCCG10GENIChomozygous714617123